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  • Internal

    £22,000
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    We are hiring for spots in April and across our Summer intake this year. We have come into 2021 in a very strong position and are excited to bring the next group of graduates through our training programme to start an exciting career within recruitment!

    About Skills Alliance

    Skills Alliance Group is a Global Life Science, Medical Device & Technology, and Animal Health recruitment company encompassing three business units: SA Executive, SA Staffing & SA Consulting.

    For the past 15 years, we have been providing innovative and bespoke recruitment solutions that facilitate our clients need to hire exceptional talent quickly. To date we count many of the leading pharmaceutical, biotechnology, biopharma and CROs as our partners, and we are proud to be contributing to the discovery, development and distribution of safe and effective therapeutics across the globe.

    If you are a graduate and unsure on what recruitment company or sector to join pharma is one of, if not the top and most stable sector to be working in right now. 2020 was a record year for us in regards to promotions and personal billing achievements, we made zero redundancies with the virus and actually grew our global headcount by 20%.

    The core values of our business dictate and shape every decision we make. We therefore behave with agility, continuously improve and are always proactive in every action we take. We also like to have a lot of fun on the way.

    Why Skills Alliance?

    We have a vibrant office based in the City of London that is growing rapidly and have continued to grow through COVID. We come to work every day to do something we love and are genuinely passionate about the industry that we work in. We always conduct employee engagement surveys and the one thing that all of our staff say they love the most about us is the people and culture. We have an amazing culture that we have worked hard on creating. We also work only mid to senior level appointments as well as retained searches which means higher fees and in return the opportunity to earn much more commission.

    What we offer:

    • Competitive basic salary and potential to earn some serious cash: we offer £22,000 on start increasing to £25,000 at 6 months. You can earn up to £60,000 in your first year and over £100,000 in your second year
    • The perks: A fun and extremely buzzy office with perks such as dress down Fridays, beers in the office on Fridays with an early finish, a summer party, huge Christmas party, loads of social events and monthly Director drinks.
    • Benefits: such as flexi time, working from home, private health insurance, corporate gym membership, office meditation sessions, health & wellness programme, duvet days, birthdays off and a generous vacation allowance.
    • Incentives: such as lunch clubs, 2x yearly holiday incentives (previous destinations include Croatia, Ibiza, South of France & Budapest, fantasy recruitment league, the £100K club and quarterly team incentives.
    • 5* Dining: We love a lunch club and the opportunity to have a ½ day at work followed by an all-expenses paid lunch at some of the top restaurants in London
    • Career progression: based on meritocracy. We believe in promoting on merit and not tenure. Promotion to consultant within 6 months and senior consultant 12 months
    • Uncapped commission: structure up to 30% and no cap at all on how much you actually make. you also earn commission from day one.
    • Learning and Development: a supportive and structured environment which includes weekly training delivered by our Global Learning Development Manager and Senior Management Team as well as retainer training directly from our CEO
    • International office relocation: for people who want to work in our other offices (New York, Seattle, Newport Beach and Zurich)

     

    The Trainee Training Academy

    We have a strong track record in training and developing our staff to the highest level and our learning and development function is headed up by somebody who has over the years produced many top billers. As a new employee you will go through an initial 4-week intensive programme learning about the recruitment sector and your market. Every employee will have training throughout their career to ensure that you will always have access to the best support and development.

    The Trainee Academy is where the basics of Recruitment are covered and the participants can learn and practice in a safe environment before being exposed to candidates and clients, peer to peer mentoring, call coaching and modelling success on the companies’ high performers. There then follows psychometric self-development assessment and continual one to one mentoring

    Duties of a Graduate Recruitment Consultant:

    • Business Development and building business relationships as well as cold calling
    • Headhunting and identifying suitable candidates
    • Negotiating and objection handling
    • Qualifying candidates and building candidate networks
    • Arranging and preparing candidates for interviews
    • Lead & referral generating
    • Learning to become an expect in your market

    What skills do you need?

    • A minimum of a bachelor’s degree – Graduating in 2020 or 2021
    • Strong communication skills and the ability to develop new business relationships
    • Ability to listen, learn and apply new ideas quickly
    • A confident personality and will not be afraid to get on the phones
    • Previous sales experience would be highly advantageous
    • Ability to achieve set targets and working to deadlines.
    • Entrepreneurial, ambitious and enjoy a fast paced, but challenging atmosphere.
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    Skills Alliance is a fast growing, specialist life science recruitment firm with offices in London, New York, Seattle, Newport Beach and Zurich. Due to client demand and subsequent business growth, we are looking to hire ambitious, driven and self-motivated Principal Consultants to build on our current success and become future business leaders.

    We are open to consultants from any specialist sector, for example energy or finance who are now looking for a change in market and the opportunity to develop with a fast growing International business.

    We offer uncapped commission, good basic salaries, career development based on ability rather than tenure, individual and team incentives and a very entrepreneurial work atmosphere. The business offers a specialist, boutique feel but with the opportunity to develop your career quickly by working with a highly experienced and internationally recognised senior management team.

    As a new employee you will benefit from the following:

    • The ability to work with market leading consultants and work on and influence top tier executive search work
    • Travel across Europe and Internationally
    • Monthly, quarterly and bi-yearly incentives and holidays
    • Freedom to share and implement your own ideas

    Your primary duties will be focused on building up your specialist vertical market, becoming a subject matter expert and developing your brand and identity within Skills Alliance and the industry. On a day to day basis the core duties for this position will involve:

    • To drive growth and develop the specified vertical market for Skills Alliance on a Pan European basis.
    • You will act as a 360 consultant and as such will be responsible for both client and candidate development.
    • To achieve consistent and rising revenue generation within the specified vertical of the Life Sciences / Pharmaceutical sector.
    • The successful candidate will be expected to offer constructive, entrepreneurial and forward thinking ideas and concepts to assist in the development and growth of Skills Alliance as a leading Global Pharmaceutical Recruitment business.
    • To attend Industry specific conferences and symposia on behalf of Skills Alliance and represent the brand and organization. Build talent-pools of candidate resumes and establish yourself within a vertical market.
    • Screen resumes and qualify potential candidates about suitable job vacancies.
    • Develop leads for new business and conduct business development with new clients within the target vertical by agreeing working agreements and establishing terms of business with Life Sciences / Pharmaceutical companies.

    Additional requirements

    • Ideally you will have a minimum of a University degree
    • Strong communication skills and the ability to build relationships with a variety of customers.
    • At senior level, we would be looking at full 360 recruitment experience with an ability to demonstrate client and candidate acquisition.
    • An ability to listen, learn and apply new ideas quickly
    • Most importantly, we want to hear from people who always strive to be the best at anything they apply themselves to do.

     

    If you are interested in a confidential discussion, please do apply to this job advert with a CV and cover letter explaining the reasons for your interest in the position.

  • Clinical Operations

    £50 - £80 per hour
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    The Global Clinical Sciences and Operations department, are looking for an individual to fill the position of Senior Clinical Project Manager.

    Start date:as soon as possible
    Duration: 12 months –

    JOB SUMMARY
    Accountable for the delivery of one or more studies from protocol through to study report and archiving. These can be all types of study from First in Human to Phase IV Accountable for managing the interface between the company, Phase 1 Units, CROs and other vendors to ensure assigned studies are delivered according to contract specifications, with high quality, on time and on budget.

    Accountable for leading the internal and Joint Clinical Study team; lead study specific decision-making, develop strategies for increasing study efficiencies and co-ordinate issue detection, resolution and, where necessary, escalation to the Program Delivery Leads.

    The level of CPM assigned to a project (either CPM or Senior CPM) will be dependent on study complexity and type (e.g. First in Human studies), scope, size and geography.

    Senior CPMs will be accountable for more complex studies and/or those with high visibility such as pivotal trials or challenging POC studies.


    MAJOR ACCOUNTABILITIES
    • Lead one or more multi-functional, Clinical Study Team(s) / Joint Clinical Study teams, tailoring the communication interface to ensure effective co-ordination and communication within and across the internal and CRO/Phase 1 Unit teams.

    • If a Clinical Pharmacology study, ensure selection of the optimal Phase I Unit within or outside the SPI framework depending on the specialist need of the study.

    • At the study kick-off meeting, articulate study scope, goals, and expectations of Sponsor to the CRO/Phase 1 Unit and ensure any relevant information that may impact the set-up of the trial is highlighted and accounted for in the trial planning.

    • Creates, or contributes, to detailed planning of the study timelines, defining critical path, and enabling seamless, and timely, access to bioanalytical and/or safety data for review meetings and so allowing prompt decision making. Such as for Safety Monitoring/Data Monitoring Committees, planned Interim Analyses, and final data reporting for Results Interpretation Meetings and final CSR.

    • Ensure that the scope, and all tasks and responsibilities for a study, are appropriately reflected in all study contracts and amendments. Ensure that scope changes are tracked, appropriately endorsed, and reflected in contract amendments before implementation of activities by the CRO/Phase 1 Unit.

    • Review and challenge CRO/Phase 1 Unit strategy and plans, if appropriate.

    • Demonstrate robust oversight of sponsor delegated activities by regularly reviewing CRO/Phase 1 Unit performance through use of KPIs, metrics and deliverables, with a focus on trial subject safety, data quality, and critical activities that might delay the project or impact budget.

    • Ensure a risk assessment is performed and a Risk Mitigation Plan is set-up at the beginning of the study and maintained by the partner CRO.

    • Regularly monitor and assess the appropriateness of the risk mitigation plan with the Clinical Study Team(s) / Joint Clinical Study teams and ensure that the cause, impact, remedial actions & preventative steps are assessed for any issues identified to avoid recurrence. Findings, including mitigation plans, to be discussed with the CRO and communicated to all appropriate internal and external stakeholders.

    • Become familiar with the competitive landscape; engage with KOLs, investigational sites, patient advocacy groups and other relevant organizations.

    • Understand, manage, track and ensure accuracy of study budgets in systems, including the forecast and accrual information.

    • For assigned studies, work closely with the respective Program Delivery Leads, and other team members and stakeholders as required, to serve as the key internal clinical operations contact whilst keeping the PDL updated on all study issues.

    • Closely cooperate with OC&SP and, if applicable, relevant committees/governance bodies and/or CQA regarding the performance and quality of work received from the CROs/Phase 1 Units and other vendors.

    • Collaborate with members of Clinical Study Team(s) / Joint Clinical Study teams to develop clinical trial protocols, protocol amendments, and other relevant study documents by providing input and/or approval as defined in SOPs and, if applicable, Strategic Partnership (SP) documents. Ensure that these documents are appropriately updated, e.g. in case new safety information or other change in scope.

    • Work with CRO partners to define a study specific monitoring strategy. Review Monitoring Plans, and CRA generated reports (as appropriate).

    • Provide input to aid in the development of the clinical database, and clinical operations focused review of the clinical database specifications during set-up, and support data cleaning and data evaluation meetings and Results Interpretation Meetings (RIMs).

    • Support Data cleaning and data evaluation meetings (DEM) and Results Interpretation Meetings (RIMs) • Support conduct of Data Monitoring Committee (DMC)/Safety Monitoring Committee (SMC) review meetings.

    • Ensure that Clinical Study Reports (CSRs) meet the objectives of the trial and correctly reflect the data and the study conduct, in collaboration with the study team members.

    • Lead lessons learned meetings as appropriate for assigned studies with internal and CRO team members.

    • Ensure quality and adherence to the relevant SOPs, GCP, regulatory guidelines and working practices.

    • Support any audit/inspection activities and support CQA to ensure that result findings from audits/inspections are appropriately addressed in a timely manner.

    • Asia Specific – support any Regulatory Authority consultation activities.sm

    • Provide study specific training for internal (i.e. Sponsor) and external (i.e. CRO, vendors, investigators) team members.

    • Identify issues/gaps in processes and interfaces with other groups and departments and contribute to developing recommendations for resolution. Contribute to process improvement initiatives, and share best practice experiences with line manager, peers and Partner CROs.

    • Visit investigational sites and Phase 1 Units to build and maintain relationships as well as to understand opportunities and challenges to study conduct, including enrollment, when needed for assigned clinical studies.

    • Travel including overnight stays- possibly global – required.

    • A Senior CPM is expected to mentor other colleagues, present clinical trial related information internally or to an external audience as appropriate.

    • A Senior CPM may be assigned to more complex studies and/or those with high visibility such as pivotal trials or challenging POC trials, or multiple studies running in parallel.

    • Perform other tasks as deemed necessary by the Company.

    EDUCATION & QUALIFICATION
    Minimum BA/BSc

    At least three years’ relevant experience in clinical development including team leadership.

    Experience or capability to manage in-house and/or outsourced regional or global Phase 1, 2 or 3 studies (First in Human to multicenter clinical studies) from study start-up to study report completion.

    *A SrCPM must have substantial experience in study management in different indications and proven ability to manage complex multinational studies or multiple simultaneous studies from start to end.*

  • Clinical Operations

    £60000 - £70000 per annum, Bonus + benefits
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    Great opportunity for a Study Manager or Senior Study Manager to join a niche Bitoech working in advanced therapies. The role would be home-based initially with some travel to an office when normality resumes!

    The role is with a niche company who are very innovative and have exciting science. They company are growing quickly and have advanced therapies trials in early stages across several indications. This would be working at the cutting edge of research.

    The position is a wide ranging one given the size of the team. They need an autonomous Clinical Study Manager who is keen to work in both science and operations. Early phase project management expeirence would be preferable.

    This is a permanent and full-time role. The role would be home-based initially with some travel to the office in the long-run. They offer an excellent salary + bonus.

    Skills Alliance are the preferred supplier for this role. Please contact Mark Anderson for more details – +44 207 220 6209 or click apply now.

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    Job Overview
    The Senior Analyst, PV Vendor & Alliance Management (PVAM) is responsible for supporting the activities performed within this group. This position assists the leaders of PV Vendor & Alliance Management in the effective oversight of outsourced activities, monitoring service provider performance and compliance with their contractual obligations. This position will interact with PV staff, staff in other departments and with
    service providers performing activities supporting the global PV system.

    Essential Functions

    • Acts as an external training coordinator and coordinates Adverse Event reporting training to service providers supporting programs
    • Coordinates PV review of project materials for programs which have the potential to generate safety information
    • Coordinates implementation of Safety Reporting plans for programs with the potential to generate safety information
    • Maintains a tracker of all programs for which the PV review of materials has been coordinated.
    • Coordinates access (on-boarding / off-boarding) to network and the global safety database for service provider staff, as appropriate.
    • Monitors the PVAM mailbox and responds to queries.
    • May assist with update to Service Provider Oversight Plans.
    • May assist with update to PVAM controlled documents.
    • Supports collection of information required to update designated sections of the PSMF.
    • Facilitates service provider on-boarding and ongoing training for products, data bases and SOPs and ensures service providers have access to all current reference materials appropriate to their remit.
    • Coordinates PVAM departmental meetings and is responsible for maintenance of the PVAM tracker
    • Undertakes additional projects, as assigned, in support of PV or other business goals.

    Required Knowledge, Skills, and Abilities

    • Knowledge of and experience with EU and US FDA PV regulations
    • In depth knowledge of pharmacovigilance activities and processes, with a preference for experience in more than one PV functional area
    • Knowledge of current and emerging regulatory requirements and expectations including EMA GVP Modules, FDA IND and NDA reporting requirements, global risk management requirements, ICH, CIOMS.
    • Experience interacting with service providers or external business partners
    • Excellent teamwork and interpersonal skills are required with ability to effectively collaborate with internal and external contacts, building strong sustainable relationships
    • Excellent oral and written communication skills, demonstrating professional maturity, confidence and competence
    • Ability to work effectively within a matrix organization to achieve desired outcomes
    • Track record of effective decision-making; makes good business decisions and analyses problems from multiple perspectives
    • Ability to work across cultures, including in a virtual environment
    • Proficiency with MS Office (e.g. Word, Excel, PowerPoint, Outlook)
    • Proven ability to demonstrate values

    Required/Preferred Education and Licenses

    • Health Care Professional Degree or Life Science Degree, or equivalent experience required
    • A minimum of 3 years’ experience in pharmaceutical safety required
    • Experience in a role involving vendor partnership/relationship management responsibilities preferred
  • Clinical Operations

    £60000 - £80000 per annum, bonus + shares + benefits
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    I am partnered with an exciting Oncology Biotech in Central London who have a unique model and a strong pipeline.

    This Biotech works specifically in Oncology and have a number of early phase assets, they work in a range of areas within the Oncology field. They have excellent funding and are a very secure organisation despite being relatively small. They plan to remain quite small and outsource the trials to CRO. They have a unique model and are doing exciting work in the cancer field.

    They are recruiting for a Senior Clinical Trial Manager to join the team and need a very experienced and accomplished Project/Study Manager, Ideally with several years working at senior trial management level. Pharma/Biotech experience, significant Oncology experience and early phase (I and II ideally) is required. You are likely to be responsible for several early phase projects. They need someone who autonomous and can work in a small and dynamic team. Protocol writing would be of benefits and experience of working cross-functionally.

    This is a full-time and permanent role, it would be home-based initially and they would want someone in the office several days per week post-COVID. The office is based in Central London. There is an excellent salary and package on offer – £65-80K depending on experience + bonus + benefits + share options.

    Skills Alliance are the exclusive partner for this position, please get in touch with Mark Anderson to find out more on +44 207 220 6209 or APPLY NOW.

  • Clinical Operations

    £60000 - £80000 per annum, bonus + shares + benefits
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    I am partnered with an exciting Oncology Biotech in Central London who have a unique model and a strong pipeline.

    This Biotech works specifically in Oncology and have a number of early phase assets, they work in a range of areas within the Oncology field. They have excellent funding and are a very secure organisation despite being relatively small. They plan to remain quite small and outsource the trials to CRO. They have a unique model and are doing exciting work in the cancer field.

    They are recruiting for a Senior Clinical Trial Manager to join the team and need a very experienced and accomplished Project/Study Manager, Ideally with several years working at senior trial management level. Pharma/Biotech experience, significant Oncology experience and early phase (I and II ideally) is required. You are likely to be responsible for several early phase projects. They need someone who autonomous and can work in a small and dynamic team. Protocol writing would be of benefits and experience of working cross-functionally.

    This is a full-time and permanent role, it would be home-based initially and they would want someone in the office several days per week post-COVID. The office is based in Central London. There is an excellent salary and package on offer – £65-80K depending on experience + bonus + benefits + share options.

    Skills Alliance are the exclusive partner for this position, please get in touch with Mark Anderson to find out more on +44 207 220 6209 or APPLY NOW.

  • Regulatory

    £50 - £80 per hour
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    This is a 12 Month remote contract position working with a leading CRO based in London. They are seeking Regulatory Affairs Subject Matter Expert to serve as a periodic advisor to select Sponsors at our client. This person could be assigned to projects for their duration or may be called upon to answer ad-hoc questions as required.

    In terms of the performance and personal competencies required for the position, we would highlight the following:

    • Prefer advanced degree, such as PhD or MD with minimum 15 years combined experience in Global Regulatory Affairs and Clinical Development, in at least two therapeutic areas across phase I-IV; has a track record of successful filings.
    • An experienced leader who has successfully managed high performance cross-functional teams, worked in a matrix structure, with the ability to translate strategy into clear operational objectives.
    • Have the gravitas, confidence and executive presence to operate with business leaders. Be self-confident, but without ego. Have not only scientific credibility, but obvious business acumen.
    • Experience interfacing with regulatory agencies, thorough knowledge and understanding of regulatory requirements for pharmaceutical/biological product development and approval in more than one key region (ie. US, EU, Japan).
    • Experience with communicating the regulatory strategy, issues, and risks in written and verbal format to regulatory senior leadership team and other governing bodies.
    • Demonstrated ability to coordinate global activities and has a track record in regulatory success is important.
    • Excellent verbal and written communication skills and collaborative interpersonal skills.
  • Procurement

    $200000 - $260000 per annum
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    Skills Alliance are partnering one of the most exciting, fastest growing biotechnology start-up organizations in the US. After gaining significant investment, they are expanding operations in Massachusetts to include a new strategic procurement and supply chain management team.

    As part of this new greenfield transformation, they are seeking to recruit an experienced Procurement Lead to drive forward category strategies, sourcing projects and building stakeholder relations across their laboratory operation. You will be responsible for the Lab Services, Supplies and Equipment spend in what will be a very expansive and science-driven environment. We are considering candidates for this position at either Director, or Senior Director level within the organization (dependent on experience).

    Responsibilities:

    • Build the Lab Consumables, Equipment, and Services category/team from the ground up, ensuring that key products and services are available at the highest level of quality, efficiency, and cost.
    • Develop overall category vision, strategy, priorities, and portfolio of projects, collaborating with relevant business stakeholders to ensure effective alignment.
    • Design and implement an effective strategy for lab consumables, equipment, and service-related spend areas, collaborating with cross-functional teams to gather business requirements and market insights that support key decisions.
    • Assess options and strategies for supply chain and sourcing, and oversee plans for implementation and operationalization.
    • Develop a robust portfolio of sourcing projects to achieve year-over-year productivity and deliver cost savings targets.
    • Ensure relevant customer-centric procurement KPIs are created, implemented, and tracked.
    • Initiate, negotiate, and execute contracts and agreements for commercial terms, intellectual property, and confidentiality, working with our Legal Team to ensure compliance with all legal, ethical, and procurement standards.
    • Develop and manage key supplier relationships through appropriate programs (e.g. alliance/supplier relationship management) to enable innovation and cost reduction through mutual accountability and trust.
    • Establish category and supplier management processes, driving the value messaging of and compliance with these processes across the company
    • Support the Lab Consumables, Equipment, and Services Team by securing the appropriate sponsorship, resources, and implementation support, and providing strategic insight and access to all relevant resources and data.
    • Ensure that the team engages with and fully supports supply base and supplier management strategies, helping to identify and resolve compliance issues with respect to the usage of preferred suppliers.
    • Help to meet deliverables, as agreed upon during Category Plan development

    Required Experience:

    • Bachelor’s or Master’s degree in supply chain management, procurement operations, or related field
    • 10+ years of experience with sourcing laboratory equipment; prior experience with SME pharma/biotech companies strongly preferred
    • Prior management experience with lab consumables, equipment, and service category/spend – as well as direct management of team members – preferably within a laboratory and/or scientific environment
    • Strong leadership skills, with the ability to establish and execute new strategies and processes
    • Proven ability to manage negotiations, suppliers, and contracts
    • High-level problem-solving and analytical skills, with the ability to identify, maintain, and utilize key metrics to make data-driven decisions and make continuous improvements
    • Exceptional ability to build strong relationships, develop negotiation strategies, and influence technical, business, and operational decisions
    • Strong multitasking skills, with the ability to work on multiple, concurrent projects and adapt to changing priorities in a fast-paced, high-growth environment
    • Excellent verbal/written communication skills and attention to detail, with the ability to efficiently organize information, analyze large datasets, and present data in a clear and impactful manner
  • Procurement

    $140000 - $180000 per annum
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    Skills Alliance are partnering one of the most exciting, fastest growing biotechnology start-up organizations in the US. After gaining significant investment, they are expanding operations in Massachusetts to include a new strategic procurement and supply chain management team.

    As part of this new greenfield transformation, they are seeking to recruit an experienced Procurement Manager to drive forward category strategies, sourcing projects and building stakeholder relations across their laboratory operation. You will be responsible for the Lab Services, Supplies and Equipment spend in what will be a very expansive and science-driven environment. We are considering candidates for this position at Manager to Associate Director level (dependent on experience).


    Responsibilities:

    • Manage the continuous sourcing of lab equipment and services, ensuring uninterrupted supply.
    • Create and execute effective strategies for lab equipment and services-related spend areas, collaborating with cross-functional teams and relevant stakeholders to gather business requirements and market insights to drive decisions.
    • Collaborate with stakeholders to consolidate volumes and assist with instrumentation maintenance coverage selection.
    • Assess options and strategies for supply chain and sourcing, and oversee plans for implementation and operationalization.
    • Support Buy versus Lease decisions.
    • Initiate, negotiate, and execute contracts and agreements for commercial terms, intellectual property, and confidentiality, working with our Legal Team to ensure compliance with all legal, ethical, and procurement standards.
    • Build effective spend management tools to drive effective decisions regarding the total cost of ownership and asset utilization.
    • Develop and manage key supplier relationships through appropriate programs.
    • Collaborate with finance to streamline the budget/forecasting process relating to third-party spend.


    Required Experience:

    • Bachelor’s or Master’s degree in supply chain management, laboratory technology, or related field.
    • 5+ years of experience with sourcing laboratory equipment; prior experience with SME pharma/biotech companies strongly preferred.
    • 3+ years of experience with managing lab equipment and service category/spend, preferably within a laboratory and/or scientific environment.
    • Proven ability to manage negotiations, suppliers, and contracts.
    • Strong analytical, strategic, and critical thinking skills.
    • Excellent verbal/written communication skills and attention to detail, with the ability to efficiently organize information, analyze large datasets, and present data in a clear and impactful manner.
    • High-level ability to build strong relationships and influence technical, business, and operational decisions.
    • Strong multitasking skills, with the ability to work on multiple, concurrent projects and adapt to changing priorities in a fast-paced, high-growth environment.
  • Clinical Operations

    £60000 - £75000 per annum, Bonus + benefits
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    Great opportunity for an experienced Clinical Project Manager or Study Manager to join a niche Bitoech working in Oncology. The role would be home-based initially with some travel to the office when normality resumes.

    The role is with a niche company who are very innovative and work specifically in Oncology. The company is growing quickly and have exciting early phase programs ongoing. This would be working at the cutting edge of research with a great team who are looking to make a real impact on patients’ lives.

    The position is a wide ranging one given the size of the team. They need an autonomous Clinical Study Manager who is keen to work in both science and operations. Early phase project management expeirence and Oncology trial management is essential for this role.

    This is a permanent and full-time role. The role would be home-based initially with some travel to the London office further down the line. They offer an excellent salary in the region of £60-75K depending on expeirence + bonus + benefits.

    Skills Alliance are the exclusive partner for this role. Please contact Mark Anderson for more details – +44 207 220 6209 or click “APPLY NOW”.

  • Clinical Operations

    £60000 - £80000 per annum, Excellent package
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    *PHARMA EXPERIENCE REQUIRED*

    Skills Alliance are retained on a unique opportunity with an innovative not-for-profit organisation.

    The company specialises in vaccine development to combat epidemic outbreaks such as Coronavirus and Ebola, they are a global partnership of government, civil society, philanthropic and Pharma organisations. They have a unique approach and will have a direct impact on global epidemics in the coming years. With this goal in mind, they are looking to build out the organisation and are looking for high calibre candidates who want to make a difference.

    The (Senior) R&D Project Manager will facilitate the successful delivery of several vaccine R&D projects associated with the organisation’s mission. Responsible to proactively manage all elements of each project – monitoring, scope, timelines, risk, budget and quality. They require previous R&D project management experience, ideally managing projects from pre-clinical to commercialisation. Cross-functional PM experience is required and experience of overseeing vaccine projects would be a bonus.

    This is a full-time and permanent position to be based at their offices in Central London with some flexibility. They will offer a very competitive salary – circa £60-80K depending on experience + full benefits package.

  • Clinical Operations

    £50000 - £60000 per annum, Bonus + benefits
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    Great opportunity for an experienced Senior / Lead CRA or Junior Study Manager to join a niche Bitoech working in advanced therapies. The role would be home-based initially with some travel to an office when normality resumes.

    The role is with a niche company who are very innovative and have had excellent results from early phase trials. The company is growing quickly and have advanced therapies trials that are progressing well. This would be working at the cutting edge of research.

    The position is a wide ranging one given the size of the team. They need an autonomous Senior / Lead CRA or Junior Study Manager who is keen to work in both science and operations. Early phase Lead CRA or project management expeirence would be preferable and some international experience.

    This is a permanent and full-time role. The role would be home-based initially with travel to the office in the London area when they can return to the office. They offer an excellent salary – circa £50-60K + bonus.

    Skills Alliance are the preferred supplier for this role. Please contact Mark Anderson for more details – +44 207 220 6209 or click apply now.

  • Clinical Operations

    £60000 - £85000 per annum, Bonus + benefits
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    Great opportunity for an experienced Clinical Project Manager or Study Manager to join a niche Bitoech working in Oncology. The role would be home-based initially with some travel to the office when normality resumes.

    The role is with a niche company who are very innovative and work specifically in Oncology. The company is growing quickly and have exciting early phase programs ongoing. This would be working at the cutting edge of research with a great team who are looking to make a real impact on patients’ lives.

    The position is a wide ranging one given the size of the team. They need an autonomous Senior Clinical Study Manager who is keen to work in both science and operations. Early phase project management expeirence and Oncology trial management is essential for this role.

    This is a permanent and full-time role. The role would be home-based initially with some travel to the London office further down the line. They offer an excellent salary in the region of £60-85K depending on expeirence + bonus + benefits.

    Skills Alliance are the exclusive partner for this role. Please contact Mark Anderson for more details – +44 207 220 6209 or click “APPLY NOW”.

  • Clinical Operations

    £60000 - £90000 per annum, bonus + shares + benefits
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    Share

    I am partnered with an exciting Oncology Biotech in Central London who have a unique model and a strong pipeline.

    This Biotech works specifically in Oncology and have a number of early phase assets, they work in a range of areas within the Oncology field. They have excellent funding and are a very secure organisation despite being relatively small. They plan to remain quite small and outsource the trials to CRO. They have a unique model and are doing exciting work in the cancer field.

    They are recruiting for a Senior Clinical Trial Manager to join the team and need a very experienced and accomplished Project/Study Manager, Ideally with several years working at senior trial management level. Pharma/Biotech experience, significant Oncology experience and early phase (I and II ideally) is required. You are likely to be responsible for several early phase projects. They need someone who autonomous and can work in a small and dynamic team. Protocol writing would be of benefits and experience of working cross-functionally.

    This is a full-time and permanent role, it would be home-based initially and they would want someone in the office several days per week post-COVID. The office is based in Central London. There is an excellent salary and package on offer – £65-90K depending on experience + bonus + benefits + share options.

    Skills Alliance are the exclusive partner for this position, please get in touch with Mark Anderson to find out more on +44 207 220 6209 or APPLY NOW.

  • Clinical Operations

    £50000 - £60000 per annum, excellent package
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    Share

    A rare opportunity to join a fast growing Advanced Therapies focused Biotech. This is a permanent Clinical Trial Manager or Clinical Study Manager role based in the London area.

    This exciting and innovative Biotech company are at early stages with trials working in advanced therapies. They are expanding at present and will offer great long-term prospects. The company are looking for an experienced Junior Study Manager or Clinical Trial Manager, this would be working on interesting studies from phase I-III. They require a clinical trial management experience, ideally experience in early phase, complex TAs and experience of working with sites. They have multiple programs ongoing and have a global presence.

    This is a full-time and permanent position. It is office-based in the London area with flexibility to work from home (home-based during the pandemic). They offer an excellent salary and package around GBP 50-60K depending on experience + bonus + extensive benefits.

    Skills Alliance are the preferred supplier for this new CPM / CTM position. For more details please call Mark Anderson on 0207 220 6209 or click apply now.

  • Clinical Operations

    £60000 - £80000 per annum, Excellent package
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    Share

    *PHARMA EXPERIENCE REQUIRED*

    Skills Alliance are retained on a unique opportunity with an innovative not-for-profit organisation.

    The company specialises in vaccine development to combat epidemic outbreaks such as Coronavirus and Ebola, they are a global partnership of government, civil society, philanthropic and Pharma organisations. They have a unique approach and will have a direct impact on global epidemics in the coming years. With this goal in mind, they are looking to build out the organisation and are looking for high calibre candidates who want to make a difference.

    The (Senior) R&D Project Manager will facilitate the successful delivery of several vaccine R&D projects associated with the organisation’s mission. Responsible to proactively manage all elements of each project – monitoring, scope, timelines, risk, budget and quality. They require previous R&D project management experience, ideally managing projects from pre-clinical to commercialisation. Cross-functional PM experience is required and experience of overseeing vaccine projects would be a bonus.

    This is a full-time and permanent position to be based at their offices in Central London with some flexibility. They will offer a very competitive salary – circa £60-80K depending on experience + full benefits package.

  • Clinical Operations

    £65000 - £75000 per annum, Bonus + benefits
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    Great opportunity for an experienced Study Manager or Senior Study Manager to join a niche Bitoech working in advanced therapies. The role would be home-based initially with some travel to an office when normality resumes.

    The role is with a niche company who are very innovative and have exciting science. They company are growing quickly and have advanced therapies trials in early stages across several indications. This would be working at the cutting edge of research.

    The position is a wide ranging one given the size of the team. They need an autonomous Senior Clinical Study Manager who is keen to work in both science and operations. Early phase project management expeirence would be preferable and global experience.

    This is a permanent and full-time role. The role would be home-based initially with some travel to the office in the long-run. They offer an excellent salary + bonus.

    Skills Alliance are the preferred supplier for this role. Please contact Mark Anderson for more details – +44 207 220 6209 or click apply now.

  • Manufacturing

    Competitive
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    Pour le compte d’une société biopharmaceutique avec un site de production dans le canton de Neuchâtel, Skills Alliance est à la recherche d’un QA Expert (CDI) qui sera responsable de l’Assurance Qualité tout au long des processus de production et de libération des lots.

    Responsabilités:

    • Participer aux activités quotidiennes liées à la revue des dossiers de lot et des données associées pour la libération des lots;
    • “Change control” selon les procédures, méthodes, systèmes qualité et des dossiers règlementaires applicables;
    • Maintenir le ”mapping” organisé des variants de procédés (les codes produits);
    • Résolution des problèmes et des causes à l’origine des déviations et CAPA;
    • Audits GMP internes;
    • Implémentation des projets du site en accord avec les exigences réglementaires et du département Qualité.

    Profil recherché:

    • Diplôme en Ingénierie, Biotechnologie, Pharmacie ou Qualité;
    • 3 années d’expérience en Assurance Qualité / Contrôle Qualité;
    • Connaissance des réglementations FDA, EMA, ICH, Pharmacopées;
    • Connaissance des normes système qualité;
    • Maitrise du français et niveau d’anglais professionnel (B2).

    Pour recevoir plus d’informations sur ce poste, veuillez postuler ou contacter Khephren Mongongu au +41 43 508 29 16.

  • Clinical Operations

    £60000 - £70000 per annum, Bonus + benefits
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    Share

    Great opportunity for a Study Manager or Senior Study Manager to join a niche Bitoech working in advanced therapies. The role would be home-based initially with some travel to an office when normality resumes!

    The role is with a niche company who are very innovative and have exciting science. They company are growing quickly and have advanced therapies trials in early stages across several indications. This would be working at the cutting edge of research.

    The position is a wide ranging one given the size of the team. They need an autonomous Clinical Study Manager who is keen to work in both science and operations. Early phase project management expeirence would be preferable.

    This is a permanent and full-time role. The role would be home-based initially with some travel to the office in the long-run. They offer an excellent salary + bonus.

    Skills Alliance are the preferred supplier for this role. Please contact Mark Anderson for more details – +44 207 220 6209 or click apply now.

  • Clinical Operations

    £60000 - £90000 per annum, bonus + shares + benefits
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    Share

    I am partnered with an exciting Pharma client in the London area to help build out a new team in Oncology.

    This Pharma works across a range of areas but is investing a lot in Oncology at present. They are a fantastic organisation who offer excellent development opportunities. Given their success in bringing products to market, rate of growth and the new team, this is a rare and exciting proposition. This is working in their Oncology business unit.

    They are recruiting for a Senior Clinical Study Manager to join the team and need a very experienced and accomplished Oncology Project/Study Manager.. Pharma/Biotech experience is preferred and significant Oncology experience is required.

    This is a full-time and permanent role, it would be home-based initially and they would want someone in the office several days per week post-COVID. The office is based in the London area. There is an excellent salary and package on offer – £65-75K depending on experience + bonus + benefits + share options.

    Skills Alliance are the exclusive partner for this position, please get in touch with Mark Anderson to find out more on +44 207 220 6209 or APPLY NOW.

  • Clinical Operations

    £60000 - £90000 per annum, bonus + shares + benefits
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    Share

    I am partnered with an exciting Oncology Biotech in Central London who have a unique model and a strong pipeline.

    This Biotech works specifically in Oncology and have a number of early phase assets, they work in a range of areas within the Oncology field. They have excellent funding and are a very secure organisation despite being relatively small. They plan to remain quite small and outsource the trials to CRO. They have a unique model and are doing exciting work in the cancer field.

    They are recruiting for a Senior Clinical Trial Manager to join the team and need a very experienced and accomplished Project/Study Manager, Ideally with several years working at senior trial management level. Pharma/Biotech experience, significant Oncology experience and early phase (I and II ideally) is required. You are likely to be responsible for several early phase projects. They need someone who autonomous and can work in a small and dynamic team. Protocol writing would be of benefits and experience of working cross-functionally.

    This is a full-time and permanent role, it would be home-based initially and they would want someone in the office several days per week post-COVID. The office is based in Central London. There is an excellent salary and package on offer – £65-90K depending on experience + bonus + benefits + share options.

    Skills Alliance are the exclusive partner for this position, please get in touch with Mark Anderson to find out more on +44 207 220 6209 or APPLY NOW.

  • Clinical Operations

    £60000 - £90000 per annum, Bonus + benefits
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    Share

    Great opportunity for an experienced Clinical Project Manager or Study Manager to join a niche Bitoech working in Oncology. The role would be home-based initially with some travel to the office when normality resumes.

    The role is with a niche company who are very innovative and work specifically in Oncology. The company is growing quickly and have exciting early phase programs ongoing. This would be working at the cutting edge of research with a great team who are looking to make a real impact on patients’ lives.

    The position is a wide ranging one given the size of the team. They need an autonomous Senior Clinical Study Manager who is keen to work in both science and operations. Early phase project management expeirence and Oncology trial management is essential for this role.

    This is a permanent and full-time role. The role would be home-based initially with some travel to the London office further down the line. They offer an excellent salary in the region of £65-85K depending on expeirence + bonus + benefits.

    Skills Alliance are the exclusive partner for this role. Please contact Mark Anderson for more details – +44 207 220 6209 or click “APPLY NOW”.

  • Clinical Operations

    £65000 - £75000 per annum, Bonus + benefits
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    Share

    Great opportunity for an experienced Study Manager or Senior Study Manager to join a niche Bitoech working in advanced therapies. The role would be home-based initially with some travel to an office when normality resumes.

    The role is with a niche company who are very innovative and have exciting science. They company are growing quickly and have advanced therapies trials in early stages across several indications. This would be working at the cutting edge of research.

    The position is a wide ranging one given the size of the team. They need an autonomous Senior Clinical Study Manager who is keen to work in both science and operations. Early phase project management expeirence would be preferable and global experience.

    This is a permanent and full-time role. The role would be home-based initially with some travel to the office in the long-run. They offer an excellent salary + bonus.

    Skills Alliance are the preferred supplier for this role. Please contact Mark Anderson for more details – +44 207 220 6209 or click apply now.

  • Clinical Operations

    £50000 - £60000 per annum, excellent package
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    A rare opportunity to join a fast growing Advanced Therapies focused Biotech. This is a permanent Clinical Trial Manager or Clinical Study Manager role based in the London area.

    This exciting and innovative Biotech company are at early stages with trials working in advanced therapies. They are expanding at present and will offer great long-term prospects. The company are looking for an experienced Junior Study Manager or Clinical Trial Manager, this would be working on interesting studies from phase I-III. They require a clinical trial management experience, ideally experience in early phase, complex TAs and experience of working with sites. They have multiple programs ongoing and have a global presence.

    This is a full-time and permanent position. It is office-based in the London area with flexibility to work from home (home-based during the pandemic). They offer an excellent salary and package around GBP 50-60K depending on experience + bonus + extensive benefits.

    Skills Alliance are the preferred supplier for this new CPM / CTM position. For more details please call Mark Anderson on 0207 220 6209 or click apply now.

  • Clinical Operations

    £50000 - £60000 per annum, Bonus + benefits
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    Share

    Great opportunity for an experienced Senior / Lead CRA or Junior Study Manager to join a niche Bitoech working in advanced therapies. The role would be home-based initially with some travel to an office when normality resumes.

    The role is with a niche company who are very innovative and have had excellent results from early phase trials. The company is growing quickly and have advanced therapies trials that are progressing well. This would be working at the cutting edge of research.

    The position is a wide ranging one given the size of the team. They need an autonomous Senior / Lead CRA or Junior Study Manager who is keen to work in both science and operations. Early phase Lead CRA or project management expeirence would be preferable and some international experience.

    This is a permanent and full-time role. The role would be home-based initially with travel to the office in the London area when they can return to the office. They offer an excellent salary – circa £50-60K + bonus.

    Skills Alliance are the preferred supplier for this role. Please contact Mark Anderson for more details – +44 207 220 6209 or click apply now.

  • Apply

    Job
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    I am actively recruiting on behalf of a dynamic pharmaceutical company who are launching a COVID-19 Study at with intention to start by the end of Feb.

    The role will be EDC focused and will play a vital role in the supporting the clinical team as they run the remote trial. You will not be in direct contact with the patients and the calls are done remotely, they would like individuals to be open to traveling to sites (Located around the city) should COVID-19 permit at a later date but are set up to work remotely.

    800 patient study with a projected 200 patient calls a month across the team, with 3 individuals looking to be on-boarded in this time I would like talk through the role in more depth and introduce the company.

    They are paying a competitive market rate, if interested please do apply and we can book a call to disscuss this futher.

    This role does not offer sponsorship

  • Data Management

    €35000 - €40000 per annum
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    Share

    Skills Alliance recrute pour le compte de son client une biotech specialisee dans l Equipment des laboratoires un It Administrateur Systemes et reseaux

    Ceci est un contrat de 6 mois avec une possibilite de Cdi par la suite

    En tant qu administrateur vous prenez en charge les activites liees au fonctionnement et a la maintenance du reseau local de la societe de linfrastructure migration Cloud en Azur et participez a la gestion de reseau etendu de l ensemble des entites du groupe

    Vous etes responsable egalement de l installation et la maintenance du materiel informatique des appareils mobiles et des logiciels pour permettre aux utilisateurs d acceder au reseau

    Missions

    Assurer l assistance technique de premier niveau pour les questions liees aux PC materiel logiciels telecommunications et imprimantes

    Gerer Windows active directory

    Installer configurer et maintenir les serveurs et postes de travail du reseau local

    Tester et evaluer le materiel et les logiciels

    Si vous etes titulaire d un bac plus 5 en informatique et que vous disposez deja d une experience dans un environnement Windows Microsoft server switches routers firewalls TCP IP DNS Microsoft Active Directory VMWare VSphere Office 365 One Drive SharePoint Microsoft Azure ideellement 4 ans je serai ravie de recevoir votre candidature
    L utilisation de l anglais est obligatoire pour ce poste ecrit et oral

    Localisation

    Poste Base a Moirans enMontagne avec des deplacements reguliers au sein de la societe mere basee a Villiers le Bel

  • Clinical Operations

    £85000 - £95000 per annum, Bonus + benefits
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    Share

    Skills Alliance are partnered with a very exciting and growing Biotech at present to hire for an Associate Director, Clinical Operations role in London.

    The organisation are going through a period of growth due to their own ongoing trials and a partnership with a leading global Pharma. They work in complex trials across phases I-III and work in areas of unmet medical need to hopefully have a big impact on patients’ lives. We have placed numerous people in their clin ops in the past three years and have had great feedback. They are UK based but with a global footprint.

    ASSOCIATE DIRECTOR, CLINICAL OPERATIONS – circa £85-95K

    Senior role reporting to the Global Head of Clin Ops. Line management of a group of 10-12 clin ops staff and operational responsibility including strategy, also program oversight. Strong stakeholder management required and experience in Biotech/Pharma. Significant line management experience of clin ops teams required.

    This is a permanent and full-time role, based in Central London. They will offer an excellent salary and package.

    Please get in touch with Mark Anderson for more info – 0207 220 6209 or Apply now.

  • Clinical Operations

    £75000 - £85000 per annum, Bonus + benefits
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    Share

    Skills Alliance are partnered with a very exciting and growing Biotech at present to hire for a Clinical Program Manager role in London.

    The organisation are going through a period of growth due to their own ongoing trials and a partnership with a leading global Pharma. They work in complex trials across phases I-III and work in areas of unmet medical need to hopefully have a big impact on patients’ lives. We have placed numerous people in their clin ops in the past three years and have had great feedback. They are UK based but with a global footprint.

    CLINICAL PROGRAM MANAGER – circa £75-85K

    Oversight of a portfolio of complex studies, potentially around 6 or 7 in total in phases I, II and III. No line management, purely program management. Overall budget responsibility. Experience of managing complex studies/programs required and previous program management required.

    This is a permanent and full-time role, based in Central London. They will offer an excellent salary and package.

    Please get in touch with Mark Anderson for more info – 0207 220 6209 or Apply now.

  • Project Management

    £60000 - £75000 per annum, Bonus + benefits
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    Share

    Skills Alliance are partnered with a very exciting and growing Biotech at present to hire for an Senior Project Manager (cross-functional) role in London.

    The organisation are going through a period of growth due to their own ongoing trials and a partnership with a leading global Pharma. They work in complex trials across phases I-III and work in areas of unmet medical need to hopefully have a big impact on patients’ lives. We have placed numerous people in their clin ops in the past three years and have had great feedback. They are UK based but with a global footprint.

    SENIOR PROJECT MANAGER – circa 60-75K

    Cross-functional PM for one or two complex trials, with study managers reporting into this position. Matrix management, oversight of budgets and timelines for projects. Previous cross-functional experience required from Biopharma or CRO and working with complex therapy areas.

    This is a permanent and full-time role, based in Central London. They will offer an excellent salary and package.

    Please get in touch with Mark Anderson for more info – 0207 220 6209 or Apply now.

  • Clinical Operations

    £50000 - £65000 per annum, bonus + benefits
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    I am partnered with an exciting Pharma client in the London area to help build out a new team in Oncology.

    This Pharma works across a range of areas but is investing a lot in Oncology at present. They are a fantastic organisation who offer excellent development opportunities. Given their success in bringing products to market, rate of growth and the new team, this is a rare and exciting proposition. This is working in their Oncology business unit.

    They are recruiting for a Clinical Study Manager to join the team and need an experienced and accomplished Oncology Project/Study Manager.. Pharma/Biotech experience is preferred but they will consider people from CRO and significant Oncology experience is required.

    This is a full-time and permanent role, it would be home-based initially and they would want someone in the office several days per week post-COVID. The office is based in the London area. There is an excellent salary and package on offer – £50-65K depending on experience + bonus + benefits.

    Skills Alliance are the exclusive partner for this position, please get in touch with Mark Anderson to find out more on +44 207 220 6209 or APPLY NOW.

  • Clinical Operations

    £50000 - £65000 per annum, bonus + benefits
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    I am partnered with an exciting Pharma client in the London area to help grow their Infectious Disease team.

    This Pharma works across a range of areas of unmet medical need including Infectious Disease. They are a fantastic organisation who offer excellent development opportunities. Given their success in bringing products to market and rate of growth, this is a rare and exciting proposition. This is working in their Infectious Disease business unit.

    They are recruiting for a Clinical Study Manager to join the team and need an experienced and accomplished Project/Study Manager.. Pharma/Biotech experience is preferred but they will consider people from CRO. Infectious disease or vaccines experience would be a plus but not required.

    This is a full-time and permanent role, it would be home-based initially and they would want someone in the office several days per week post-COVID. The office is based in the London area. There is an excellent salary and package on offer – £50-65K depending on experience + bonus + benefits.

    Skills Alliance are the exclusive partner for this position, please get in touch with Mark Anderson to find out more on +44 207 220 6209 or APPLY NOW.

  • Commercial

    Competitive Pay + Commission Structure
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    We are currently partnered with a groundbreaking digital pathology company that is building software to accelerate pathology’s transition from microscope to images, and effectively change the way we think about cancer altogether. Our client’s proprietary software has been developed by pathologists, for pathologists, ensuring that the scientists on the front lines are getting a product that was designed from the ground up to best support their workflows.

    After a couple of successful funding rounds, they are looking to grow their commercial sales team. This opportunity in particular is for the Head of Sales for their American business. In this role, you are responsible for the commercial success in the United States. Our client is known for pushing the limits of medicine and technology, solving problems the world has never solved before, but they can’t solve medicine alone. That’s why they’re looking for curious thinkers. Big dreamers. Developers, evangelists, pathologists, and scientists. Exceptional talent to help them use great power for good and advance humankind.

    Responsibilities:

    • Develop a Regional Sales Strategy to achieve or exceed goals, metrics, and expectations.
    • Develop strong knowledge of market, accounts, and competition and industry trends in the region.
    • Communicate overall strategy with all stakeholders including service. Adapt new GTM strategies to align with evolving customer needs.
    • Monitor, analyze, and drive sales metrics and results. Manage and drive funnel growth and forecast accuracy.
    • Coach Sales Managers in executing their business and hold them accountable for their results. Develop and leverage relationships to assist the sales team in deal closure.
    • Create and sustain relationships with senior players and CxOs at major accounts.
    • Coach the Sales Managers to meet and manage customer expectations throughout the sales process. Ensure customer issues are resolved through the escalation process.
    • Coordinate execution with key internal stakeholders to support the prospect/ customer’s needs throughout the sales process.
    • Develop and practice effective coaching skills to create a high performing team. Ensure the usage of standard processes and guidelines by the team.
    • Coach Sales Managers to create winning account and deal strategies with a unified approach to the customer.
    • Build a strong regional team through hiring, succession planning, and onboarding. Set clear expectations and communicate regularly to promote understanding. Foster a culture of teamwork, transparency, and performance-oriented growth.

    Qualifications:

    • 10+ years of enterprise software sales leadership into the clinical and/ or life sciences industry. Preferably in Healthcare informatics (PACS) or in Digital Pathology.
    • Consistent and successful sales track record (i.e. over-quota performance, forecast accuracy, balanced portfolio, notable competitive wins, etc.)
    • Demonstrates superior industry knowledge on market trends, products, and competitors in the healthcare informatics/digital pathology space.
    • Executive level selling, negotiation, and facilitation skills.
    • Leadership and team building skills.
    • Degree level education or equivalent.
    • Willing to undertake significant travel.
    • Strong moral compass.

    We are trying to move quickly on this role, so please be sure to apply today! Feel free to reach out to Ryan, the account executive for this position, directly at ryan.barrett@skillsalliance.com with any questions.

  • Commercial

    Competitive Pay + Commission Structure
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    Location: Philadelphia, PA

    We are currently partnered with a groundbreaking digital pathology company that is building software to accelerate pathology’s transition from microscope to images, and effectively change the way we think about cancer altogether. Our client’s proprietary software has been developed by pathologists, for pathologists, ensuring that the scientists on the front lines are getting a product that was designed from the ground up to best support their workflows.

    After a couple of successful funding rounds, they are looking to grow their commercial sales team. This opportunity in particular is for a Sales Director for their Life Sciences business. In this role, you are responsible for the commercial success of their Pharma, CRO, and Biotech segments on the East Coast. Our client is known for pushing the limits of medicine and technology, solving problems the world has never solved before, but they can’t solve medicine alone. That’s why they’re looking for curious thinkers. Big dreamers. Developers, evangelists, pathologists, and scientists. Exceptional talent to help them use great power for good and advance humankind.

    Responsibilities:

    • Lead sales to the life sciences segments (Pharma, CROs and biotech companies) in the East Coast of US.
    • Develop and execute a successful sales strategy for rapid revenue growth and market share expansion in the assigned territories. Contribute to business growth by meeting or exceeding bookings/ orders expectations.
    • Initialize and coordinate all efforts to strategic accounts (including tender participation) to maximize the opportunity for the sale of Proscia’s life sciences portfolio.
    • Develop, maintain, and improve relations with accounts to keep or to set Proscia as the preferred supplier. Ensure continuity of the relationship and operate at the highest level in the accounts’ organizations, facilitating the executive level interfaces.
    • Accurately complete and maintain sales forecast, customer data and other records in an orderly and timely fashion (SFDC).
    • Provide active inputs into local marketing strategies.
    • Participate in monitoring and reporting on the activities of competitors, potential collaborators, as well as identifying business opportunities.

    Qualifications:

    • Bachelor’s degree with 10+ years – OR – Master’s degree with 8+ years of proven experience in software solution/ informatics sales to Life Sciences Organizations.
    • Requires extensive knowledge and experience in digital pathology, image analysis, and AI solutions.
    • Proven ability to target key accounts and management in the territory and identify market potential.
    • Ability to perform against established performance goals and metrics
    • Willingness to independently work in a non-hierarchical company
    • Ability and curiosity to learn
    • Fluent in English, verbal and written.
    • Willing to undertake significant travel.

    We are trying to move quickly on this role, so please be sure to apply today! Feel free to reach out to Ryan, the account executive for this position, directly at ryan.barrett@skillsalliance.com with any questions.

  • Commercial

    Competitive Pay + Commission Structure
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    We are currently partnered with a groundbreaking digital pathology company that is building software to accelerate pathology’s transition from microscope to images, and effectively change the way we think about cancer altogether. Our client’s proprietary software has been developed by pathologists, for pathologists, ensuring that the scientists on the front lines are getting a product that was designed from the ground up to best support their workflows.

    After a couple of successful funding rounds, they are looking to grow their commercial sales team. This opportunity in particular is for a Sales Director for their Clinical business. In this role, you are responsible for the commercial success of their Health System, Commercial Lab, and Academic Medical Center segments on the East Coast. Our client is known for pushing the limits of medicine and technology, solving problems the world has never solved before, but they can’t solve medicine alone. That’s why they’re looking for curious thinkers. Big dreamers. Developers, evangelists, pathologists, and scientists. Exceptional talent to help them use great power for good and advance humankind.

    Responsibilities:

    • Responsible for sale to the clinical segments (Commercial labs, Health Systems and Academic Medical Centers) in the East of US.
    • Develop and execute a successful sales strategy for rapid revenue growth and market share expansion in the assigned territories. Contribute to business growth by meeting or exceeding bookings/ orders expectations.
    • Initialize and coordinate all efforts to strategic accounts (including tender participation) to maximize the opportunity for the sale of Proscia’s clinical portfolio.
    • Develop, maintain, and improve relations with accounts to keep or to set Proscia as the preferred supplier. Ensure continuity of the relationship and operate at the highest level in the accounts’ organizations, facilitating the executive level interfaces.
    • Accurately complete and maintain sales forecast, customer data and other records in an orderly and timely fashion (SFDC).
    • Provide active inputs into local marketing strategies.
    • Participate in monitoring and reporting on the activities of competitors, potential collaborators, as well as identifying business opportunities.

    Qualifications:

    • At the minimum, 10 years of healthcare sales experience and 5+ years of proven experience in healthcare informatics, medical device sales with specific experience at hospital CEO/ management level.
    • Requires extensive knowledge and experience in Healthcare Informatics, preferably, digital pathology.
    • Proven ability to target key accounts and management in the territory and identify market potential.
    • Ability to perform against established performance goals and metrics.
    • Willingness to independently work in a non-hierarchical company.
    • Ability and curiosity to learn.
    • Fluent in English, verbal and written.
    • Willing to undertake significant travel.

    We are trying to move quickly on this role, so please be sure to apply today! Feel free to reach out to Ryan, the account executive for this position, directly at ryan.barrett@skillsalliance.com with any questions.

  • Clinical Operations

    £60000 - £90000 per annum, bonus + shares + benefits
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    I am partnered with an exciting Pharma client in the London area to help build out a new team in Oncology.

    This Pharma works across a range of areas but is investing a lot in Oncology at present. They are a fantastic organisation who offer excellent development opportunities. Given their success in bringing products to market, rate of growth and the new team, this is a rare and exciting proposition. This is working in their Oncology business unit.

    They are recruiting for a Senior Clinical Study Manager to join the team and need a very experienced and accomplished Oncology Project/Study Manager.. Pharma/Biotech experience is preferred and significant Oncology experience is required.

    This is a full-time and permanent role, it would be home-based initially and they would want someone in the office several days per week post-COVID. The office is based in the London area. There is an excellent salary and package on offer – £65-75K depending on experience + bonus + benefits + share options.

    Skills Alliance are the exclusive partner for this position, please get in touch with Mark Anderson to find out more on +44 207 220 6209 or APPLY NOW.

  • Supply Chain

    £400 - £500 per day
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    Skills Alliance are supporting a global pharmaceutical organisation, undertaking a significant SAP S/4 HANA migration and process tranformation. As part of this programme, they are seeking a SAP Business Systems Analyst with a strong track record across SCM modules, to support the Supply Chain Stream as part of a program of implementations.

    Note: This will be an 11-month initial contract and sits inside IR35.

    Key Responsibilities:

    • Providing SAP expert knowledge in the functional area of Supply Chain Management in response to business requirements and to co-ordinate solutions in conjunction with our IT Technical partners.
    • Provide Business Process expertise in logically analysing and documenting Business Scenarios in collaboration with a large number of stakeholders across the Business and IT.
    • Key driver of technical change between the Business and IT – drive User Requirements/Design sessions and help co-ordinate subsequent User Testing phases and implementation.
    • Act as a bridge between the Business community and the various workstreams within a highly regulated environment.
    • Coordinate the testing activities necessary to ensure the smooth deployment of the system.
    • Support the preparation for operational readiness and work with the EMEA SCM team (affiliates, central teams and internal Manufacturing Plants) to coordinate these activities.
    • Support the affiliates and the Enterprise Master Data team in data preparation and load.
    • Support the cutover of activities for go live.
    • Support Post go live activities.


    Required Experience:

    • 5+ years SAP Supply Chain experience preferably in a regulated private-sector industry (pharmaceuticals, financial services, oil & gas).
    • Experience in SAP deployment life cycle – design, configuration, test, data conversion.
    • Experience working on large scale SAP landscapes.
    • A background helping to manage offshore partners, ensuring they deliver in terms of quality and on time.
    • Understanding of global templates across multiple countries
    • A flair for systems and willingness to learn new systems quickly as a self-starter
    • Willingness to travel on occasion when international conditions next permit.

    Required Qualifications:

    • Formal SAP and SAP SCM certifications highly desirable
    • Eligible to work in the UK as a contractor
    • Initially the role will be 100% remote, however some travel to the office in Surrey may be required after Covid restrictions lift.
  • Tech Ops

    €80 - €95 per hour
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    Great opportunity for a Process Engineer to join a leading Pharmaceutical company in Switzerland on a contract basis. This would initially be for 6 months, with likely extensions at the end of that period.

    This opportunity is within the Process Engineering team, focusing on the process planning and design of Upstream and Downstream equipment in a biopharmaceutical plant setting. As the project develops, you will be responsible for the conception, planning, construction supervision, commissioning, and qualification to handover to the customer.

    Key requirements for the role include:

    • Prior experience within a Biopharmaceutical / Biotech environment
    • Experience with Upstream and/or downstream process equipment
    • Process design experience, including P&ID’s, Process flow diagrams (PFD’s)
    • Experience working within GMP environment.

    If you would like to learn more, please apply now or reach out to Josh Taylor at Skills Alliance

  • Clinical Operations

    £65000 - £75000 per annum, Bonus + benefits
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    Great opportunity for an experienced Study Manager or Senior Study Manager to join a niche Bitoech working in advanced therapies. The role would be home-based initially with some travel to an office when normality resumes.

    The role is with a niche company who are very innovative and have exciting science. They company are growing quickly and have advanced therapies trials in early stages across several indications. This would be working at the cutting edge of research.

    The position is a wide ranging one given the size of the team. They need an autonomous Senior Clinical Study Manager who is keen to work in both science and operations. Early phase project management expeirence would be preferable and global experience.

    This is a permanent and full-time role. The role would be home-based initially with some travel to the office in the long-run. They offer an excellent salary + bonus.

    Skills Alliance are the preferred supplier for this role. Please contact Mark Anderson for more details – +44 207 220 6209 or click apply now.

  • Clinical Operations

    £60000 - £70000 per annum, Bonus + benefits
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    Great opportunity for a Study Manager or Senior Study Manager to join a niche Bitoech working in advanced therapies. The role would be home-based initially with some travel to an office when normality resumes!

    The role is with a niche company who are very innovative and have exciting science. They company are growing quickly and have advanced therapies trials in early stages across several indications. This would be working at the cutting edge of research.

    The position is a wide ranging one given the size of the team. They need an autonomous Clinical Study Manager who is keen to work in both science and operations. Early phase project management expeirence would be preferable.

    This is a permanent and full-time role. The role would be home-based initially with some travel to the office in the long-run. They offer an excellent salary + bonus.

    Skills Alliance are the preferred supplier for this role. Please contact Mark Anderson for more details – +44 207 220 6209 or click apply now.

  • Clinical Operations

    £300 - £350 per week
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    Company Overview:
    The Clinical Operations team is responsible for the execution of all Phase 1-4 clinical trials, across all therapeutic areas, around the world. In partnership with Clinical Research, Medical Affairs and other Development Operations functions, Clinical Operations ensures that all clinical trial activities are performed in accordance with applicable SOPs, company policies and regulatory guidelines to provide timely delivery of high quality clinical data to support global registration and commercialization of products. For the team based in our International Headquarters in West London, we are looking for a Clinical Trial Manager Associate to work within the Oncology therapy area.

    Essential Duties and Job Functions:
    • Provides administrative assistance in site selection, study implementation and ongoing coordination of study sites, either directly or via CROs.
    • Assist global trial managers with set-up of central labs and study vendors as required, including liaising with study management CRO to ensure site training and timely initiation.
    • Performs accompanied visits (PSSVs, SIVs, RMVs) with CRO CRAs to ensure correct study procedures according to SOPs and protocol procedures, and review of routine regulatory documents/files in compliance with protocol, regulatory requirements, SOPs, and Monitoring Plan, as required.
    • Under supervision may assist in review of protocols, informed consents, and case report forms, monitoring plans, abstracts, presentations, manuscripts and clinical study reports. May assist in compilation of investigator brochures under close supervision.
    • Review of trip reports generated by CRO CRAs
    • Communicates and collaborates with other functional groups including but not limited to Clinical Research, Regulatory Affairs, CCF, Materials and Logistics (M&L), and Drug Safety and Public Health (DSPH) to ensure efficient management of study activities.
    • Assists with the preparation and organization of international investigator meetings. Assists in preparation of safety, interim and final study reports, including resolving data discrepancies.
    • Performs administrative duties in a timely manner as assigned.
    • Travel is required up to 20-30%. (Role is currently remote due to COVID-19)

    Experience, knowledge and skills:
    • Typically requires a BS or BA in a relevant scientific discipline
    • Minimum 2 years relevant clinical trial experience in the pharmaceutical or health care industry or equivalent.
    • CRA experience preferred.
    • Oncology experience preferred but not essential.
    • Excellent verbal, written, interpersonal and presentation skills are required.
    • Must be familiar with routine medical/scientific terminology.
    • Must be familiar with Word, PowerPoint, and Excel.
    • Knowledge of FDA and/or EMEA Regulations, ICH Guidelines, and GCPs governing the conduct of clinical trials is desirable.
    • Must be able to participate in departmental or interdepartmental strategic initiative under general supervision.

    (All applicants must be happy to work through an Umbrella/PAYE as the contract will be inside IR35)

  • Clinical Operations

    €90 - €160 per hour
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    Company overview
    Commercial-stage oncology company developing a profoundly different cancer treatment therapy called tumor treating fields (TTFields) for patients with solid tumors. TTFields therapy is a non-invasive, novel, antimitotic treatment modality which utilizes proprietary technology attempting to slow or reverse tumor progression by inducing tumor cell death. Their commercialized product is approved for the treatment of adult patients with glioblastoma (GBM) in the USA, Europe and Israel. In addition this company has ongoing or completed clinical trials and is further expanding its efforts into several other solid tumor indications – non-small cell lung cancer, pancreatic cancer, ovarian cancer and other types of solid cancers.

    As the result of the launch of multiple phase II and III clinical trials we are looking for professionals who would be excited to join a fast-growing, international Clinical Operations team at our Swiss HQ.

    Senior Clinical Trial Manager
    You will be responsible for providing strategic leadership and oversight of clinical trials conducted in Europe (and other regions as needed) to ensure completion on time, within budget and of high quality in compliance with all applicable regulations, guidelines and Standard Operating Procedures. You must have a very good understanding of the project status, be able to proactively identify risks and address them appropriately (including escalation to senior management).

    Responsibilities
    The CTM responsibilities include, but are not limited to the following:
    Drive execution of the assigned clinical trial(s) on a regional level according to agreed timelines, scope and budget which includes:

    • site identification and selection
    • coordination of submissions to Competent Authorities
    • oversight of the enrollment activities on a global, country and site level
    • ensuring timely data collection, cleaning and lock
    • oversight of the clinical monitoring activities
    • oversight of CROs and other vendors

    Focus on quality

    • ensure that clinical trials are conducted in accordance with applicable regulations, ICH GCP, FDA CFR and internal Standard Operating Procedures
    • lead the preparation and follow-up after site, vendor or sponsor audits and inspections
    • be able to work with moderate supervision
    • develop and negotiate site budgets
    • prepare study reports and ensure required tools and tracking databases are kept up to date as required
    • ensure activities comply with the applicable Quality System requirements.
    • other responsibilities as assigned

    Qualifications

    • Bachelor’s degree in Nursing, Medicine or other Life Sciences, or RN degree from an accredited school
    • Minimum of 10 years’ experience working in different positions in the field of clinical trials, including CRA-level experience (both CRO and industry experience are acceptable).
    • Accredited GCP course desirable

    Knowledge/Skills

    • Fluency in English (verbal and written) and excellent communication skills
    • Strong critical thinking and problem solving skills
    • Ability to work well in a team environment
    • Strong critical thinking and problem solving skills
    • Ability to efficiently organize and prioritize work within a multifaceted framework and set deadlines
    • Excellent organizational and record-keeping skills
    • Ability to maintain excellent working relationships with a broad range of trial staff
    • Flexibility in work hours and readiness to travel abroad on a routine basis
    • Advanced computer literacy

    Happy to have remote applicants across the EMEA, with a preferance of being Swiss based, This assignment will but up to 1 FTE looking for applicants ASAP.

  • Clinical Operations

    £50000 - £60000 per annum, excellent package
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    A rare opportunity to join a fast growing Advanced Therapies focused Biotech. This is a permanent Clinical Trial Manager or Clinical Study Manager role based in the London area.

    This exciting and innovative Biotech company are at early stages with trials working in advanced therapies. They are expanding at present and will offer great long-term prospects. The company are looking for an experienced Junior Study Manager or Clinical Trial Manager, this would be working on interesting studies from phase I-III. They require a clinical trial management experience, ideally experience in early phase, complex TAs and experience of working with sites. They have multiple programs ongoing and have a global presence.

    This is a full-time and permanent position. It is office-based in the London area with flexibility to work from home (home-based during the pandemic). They offer an excellent salary and package around GBP 50-60K depending on experience + bonus + extensive benefits.

    Skills Alliance are the preferred supplier for this new CPM / CTM position. For more details please call Mark Anderson on 0207 220 6209 or click apply now.

  • Clinical Operations

    £50000 - £60000 per annum, Bonus + benefits
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    Great opportunity for an experienced Senior / Lead CRA or Junior Study Manager to join a niche Bitoech working in advanced therapies. The role would be home-based initially with some travel to an office when normality resumes.

    The role is with a niche company who are very innovative and have had excellent results from early phase trials. The company is growing quickly and have advanced therapies trials that are progressing well. This would be working at the cutting edge of research.

    The position is a wide ranging one given the size of the team. They need an autonomous Senior / Lead CRA or Junior Study Manager who is keen to work in both science and operations. Early phase Lead CRA or project management expeirence would be preferable and some international experience.

    This is a permanent and full-time role. The role would be home-based initially with travel to the office in the London area when they can return to the office. They offer an excellent salary – circa £50-60K + bonus.

    Skills Alliance are the preferred supplier for this role. Please contact Mark Anderson for more details – +44 207 220 6209 or click apply now.

  • Clinical Operations

    £60000 - £90000 per annum, bonus + shares + benefits
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    I am partnered with an exciting Oncology Biotech in Central London who have a unique model and a strong pipeline.

    This Biotech works specifically in Oncology and have a number of early phase assets, they work in a range of areas within the Oncology field. They have excellent funding and are a very secure organisation despite being relatively small. They plan to remain quite small and outsource the trials to CRO. They have a unique model and are doing exciting work in the cancer field.

    They are recruiting for a Senior Clinical Trial Manager to join the team and need a very experienced and accomplished Project/Study Manager, Ideally with several years working at senior trial management level. Pharma/Biotech experience, significant Oncology experience and early phase (I and II ideally) is required. You are likely to be responsible for several early phase projects. They need someone who autonomous and can work in a small and dynamic team. Protocol writing would be of benefits and experience of working cross-functionally.

    This is a full-time and permanent role, it would be home-based initially and they would want someone in the office several days per week post-COVID. The office is based in Central London. There is an excellent salary and package on offer – £65-90K depending on experience + bonus + benefits + share options.

    Skills Alliance are the exclusive partner for this position, please get in touch with Mark Anderson to find out more on +44 207 220 6209 or APPLY NOW.

  • Clinical Operations

    £60000 - £90000 per annum, Bonus + benefits
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    Great opportunity for an experienced Clinical Project Manager or Study Manager to join a niche Bitoech working in Oncology. The role would be home-based initially with some travel to the office when normality resumes.

    The role is with a niche company who are very innovative and work specifically in Oncology. The company is growing quickly and have exciting early phase programs ongoing. This would be working at the cutting edge of research with a great team who are looking to make a real impact on patients’ lives.

    The position is a wide ranging one given the size of the team. They need an autonomous Senior Clinical Study Manager who is keen to work in both science and operations. Early phase project management expeirence and Oncology trial management is essential for this role.

    This is a permanent and full-time role. The role would be home-based initially with some travel to the London office further down the line. They offer an excellent salary in the region of £65-85K depending on expeirence + bonus + benefits.

    Skills Alliance are the exclusive partner for this role. Please contact Mark Anderson for more details – +44 207 220 6209 or click “APPLY NOW”.

  • Medical Devices

    COMPETITIVE
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    Skills Alliance are currently partnered with a leading European specialist pharmaceutical company who is also working on Medical Device products.

    They are looking for a QA Auditor (Medical Devices) for a stand alone position on a 12 month FTC with the potential to go permanent.

    This position can be fully remote with occasional travel for audits.

    (Knowledge and/ or experience of both ISO 13485 & EU Medical Device Requirements (MDD 93/42/EEC and MDR (EU) 2017/745) is mandatory.)

    Apply now for a confidential discussion to learn more.

  • Clinical Operations

    £55000 - £65000 per annum, excellent package
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    A rare opportunity to join a growing Gene Therapies focussed Biotech. This is a permanent Clinical Study Manager role based in Central London.

    This exciting and innovative Biotech company are at early stages with trials working in advanced therapies. They are expanding at present and will offer great long-term prospects. The company are looking for an experienced Clinical Study Manager or Clinical Trial Manager, this would be working on complex and fast-paced studies from phase I-III. They require a clinical trial management experience, ideally experience in early phase, complex TAs and interntional trial management expeirence. They have multiple programs ongoing and have a global presence.

    This is a full-time and permanent position. It is office-based in the London with flexibility to work from home (home-based during the pandemic). They offer an excellent salary and package around GBP 55-65K depending on experience + bonus + extensive benefits.

    Skills Alliance are the preferred supplier for this new CPM / CTM position. For more details please call Mark Anderson on 0207 220 6209 or click apply now.

  • Project Management

    £60000 - £70000 per annum, Bonus + benefits
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    A great opportunity to join a medium-sized CRO with a great culture and low turnover. They are recruiting for PM and Senior PM roles due to organic growth and new studies.

    This company have a great track record and have been very successful during COVD where other CROs haev struggled. They are a SME CRO who are dynamic and work in very interesting areas. Studies span phases I-IV and they work in interesting areas including Oncology and Gene Therapy.

    They are recruiting for multiple roles due to new studies coming in and they need an experienced cross-functional PM who has strong budget management expeirence. It could be working on a range of studies and would be working globally. There are also opporunities to progress quickly.

    This is a permanent and full-time role. They have an office in the South East but everyone is now home-based and this can be a remote role across the UK. They will offer a very good salary – GBP 60-70K + bonus + benefits.

    Skills Alliance are the preferred supplier for this new CPM / CTM position. For more details please call Mark Anderson on 0207 220 6209 or click apply now.

  • Project Management

    £60000 - £75000 per annum, Bonus + benefits
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    Skills Alliance are partnered with a very exciting and growing Biotech at present to hire for an Senior Project Manager (cross-functional) role in London.

    The organisation are going through a period of growth due to their own ongoing trials and a partnership with a leading global Pharma. They work in complex trials across phases I-III and work in areas of unmet medical need to hopefully have a big impact on patients’ lives. We have placed numerous people in their clin ops in the past three years and have had great feedback. They are UK based but with a global footprint.

    SENIOR PROJECT MANAGER – circa 60-75K

    Cross-functional PM for one or two complex trials, with study managers reporting into this position. Matrix management, oversight of budgets and timelines for projects. Previous cross-functional experience required from Biopharma or CRO and working with complex therapy areas.

    This is a permanent and full-time role, based in Central London. They will offer an excellent salary and package.

    Please get in touch with Mark Anderson for more info – 0207 220 6209 or Apply now.

  • Clinical Operations

    £50000 - £65000 per annum, bonus + benefits
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    I am partnered with an exciting Pharma client in the London area to help grow their Infectious Disease team.

    This Pharma works across a range of areas of unmet medical need including Infectious Disease. They are a fantastic organisation who offer excellent development opportunities. Given their success in bringing products to market and rate of growth, this is a rare and exciting proposition. This is working in their Infectious Disease business unit.

    They are recruiting for a Clinical Study Manager to join the team and need an experienced and accomplished Project/Study Manager.. Pharma/Biotech experience is preferred but they will consider people from CRO. Infectious disease or vaccines experience would be a plus but not required.

    This is a full-time and permanent role, it would be home-based initially and they would want someone in the office several days per week post-COVID. The office is based in the London area. There is an excellent salary and package on offer – £50-65K depending on experience + bonus + benefits.

    Skills Alliance are the exclusive partner for this position, please get in touch with Mark Anderson to find out more on +44 207 220 6209 or APPLY NOW.

  • Clinical Operations

    £50000 - £65000 per annum, bonus + benefits
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    I am partnered with an exciting Pharma client in the London area to help build out a new team in Oncology.

    This Pharma works across a range of areas but is investing a lot in Oncology at present. They are a fantastic organisation who offer excellent development opportunities. Given their success in bringing products to market, rate of growth and the new team, this is a rare and exciting proposition. This is working in their Oncology business unit.

    They are recruiting for a Clinical Study Manager to join the team and need an experienced and accomplished Oncology Project/Study Manager.. Pharma/Biotech experience is preferred but they will consider people from CRO and significant Oncology experience is required.

    This is a full-time and permanent role, it would be home-based initially and they would want someone in the office several days per week post-COVID. The office is based in the London area. There is an excellent salary and package on offer – £50-65K depending on experience + bonus + benefits.

    Skills Alliance are the exclusive partner for this position, please get in touch with Mark Anderson to find out more on +44 207 220 6209 or APPLY NOW.

  • Clinical Operations

    £60000 - £90000 per annum, bonus + shares + benefits
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    Share

    I am partnered with an exciting Pharma client in the London area to help build out a new team in Oncology.

    This Pharma works across a range of areas but is investing a lot in Oncology at present. They are a fantastic organisation who offer excellent development opportunities. Given their success in bringing products to market, rate of growth and the new team, this is a rare and exciting proposition. This is working in their Oncology business unit.

    They are recruiting for a Senior Clinical Study Manager to join the team and need a very experienced and accomplished Oncology Project/Study Manager who would like to take on line management of a small team. Pharma/Biotech experience is preferred and significant Oncology experience is required.

    This is a full-time and permanent role, it would be home-based initially and they would want someone in the office several days per week post-COVID. The office is based in the London area. There is an excellent salary and package on offer – £65-75K depending on experience + bonus + benefits + share options.

    Skills Alliance are the exclusive partner for this position, please get in touch with Mark Anderson to find out more on +44 207 220 6209 or APPLY NOW.

  • Project Management

    £60000 - £70000 per annum, Bonus + benefits
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    A great opportunity to join a medium-sized CRO with a great culture and low turnover. They are recruiting for PM and Senior PM roles due to organic growth and new studies.

    This company have a great track record and have been very successful during COVID where other CROs have struggled. They are a SME CRO who are dynamic and work in very interesting and complex therapy areas. Studies span phases I-IV and they work in Oncology and Gene Therapy amongst other areas.

    They are recruiting for multiple roles due to new studies coming in and they need an experienced cross-functional PM who has strong budget management experience. It could be working on a range of studies and would be working globally. There are also opportunities to progress quickly.

    This is a permanent and full-time role. They have an office in the South East but everyone is now home-based and this can be a remote role across the UK. They will offer a very good salary – GBP 60-70K + bonus + benefits.

    Skills Alliance are the preferred supplier for this new CPM / CTM position. For more details please call Mark Anderson on 0207 220 6209 or click apply now.

  • Project Management

    £60000 - £70000 per annum, Bonus + benefits
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    A great opportunity to join a medium-sized CRO with a great culture and low turnover. They are recruiting for PM and Senior PM roles due to organic growth and new studies. *PHARMA EXPERIENCE REQUIRED*

    This company have a great track record and have been very successful during COVID where other CROs have struggled. They are a SME CRO who are dynamic and work in very interesting and complex therapy areas. Studies span phases I-IV and they work in Oncology and Gene Therapy amongst other areas.

    They are recruiting for multiple roles due to new studies coming in and they need an experienced cross-functional PM who has strong budget management experience. It could be working on a range of studies and would be working globally. There are also opportunities to progress quickly.

    This is a permanent and full-time role. They have an office in the South East but everyone is now home-based and this can be a remote role across the UK. They will offer a very good salary – GBP 60-70K + bonus + benefits.

    Skills Alliance are the preferred supplier for this new CPM / CTM position. For more details please call Mark Anderson on 0207 220 6209 or click apply now.

  • Project Management

    £60000 - £65000 per annum, Bonus + benefits
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    Share

    A great opportunity to join a medium-sized CRO with a great culture and low turnover. They are recruiting for PM and Senior PM roles due to organic growth and new studies. *PHARMA EXPERIENCE REQUIRED*

    This company have a great track record and have been very successful during COVID where other CROs have struggled. They are a SME CRO who are dynamic and work in very interesting and complex therapy areas. Studies span phases I-IV and they work in Oncology and Gene Therapy amongst other areas.

    They are recruiting for multiple roles due to new studies coming in and they need an experienced cross-functional PM who has budget management experience. It could be working on a range of studies and would be working globally. There are also opportunities to progress quickly.

    This is a permanent and full-time role. They have an office in the South East but everyone is now home-based and this can be a remote role across the UK. They will offer a very good salary – GBP 60-65K + bonus + benefits.

    Skills Alliance are the preferred supplier for this new CPM / CTM position. For more details please call Mark Anderson on 0207 220 6209 or click apply now.

  • Data Management

    Competitive
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    6 Month Data Management Consultancy Role: Biotechnology

    Skills Alliance are working with an exciting Biotech based in the Nordics, on a Data Management role. The client is specialised within the Immuno-Oncology space, developing disruptive immune therapies for the treatment of cancer.

    Now entering phase 2&3 trials globally they are looking for a Data Manager who can work autonomously to collate information from their providers into one central system.

    This role will allow you to work within an agile biotech and be an integral part of business growth.

    To explore further, reach out to;
    amy.mchugh@skillsalliance.com

  • Clinical Operations

    £65000 - £75000 per annum, Bonus + benefits
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    Great opportunity for an experienced Study Manager or Senior Study Manager to join a niche Bitoech working in advanced therapies. The role would be home-based initially with some travel to an office when normality resumes.

    The role is with a niche company who are very innovative and have exciting science. They company are growing quickly and have advanced therapies trials in early stages across several indications. This would be working at the cutting edge of research.

    The position is a wide ranging one given the size of the team. They need an autonomous Senior Clinical Study Manager who is keen to work in both science and operations. Early phase project management expeirence would be preferable and global experience.

    This is a permanent and full-time role. The role would be home-based initially with some travel to the office in the long-run. They offer an excellent salary + bonus.

    Skills Alliance are the preferred supplier for this role. Please contact Mark Anderson for more details – +44 207 220 6209 or click apply now.

  • Clinical Operations

    £60000 - £70000 per annum, Bonus + benefits
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    Great opportunity for a Study Manager or Senior Study Manager to join a niche Bitoech working in advanced therapies. The role would be home-based initially with some travel to an office when normality resumes!

    The role is with a niche company who are very innovative and have exciting science. They company are growing quickly and have advanced therapies trials in early stages across several indications. This would be working at the cutting edge of research.

    The position is a wide ranging one given the size of the team. They need an autonomous Clinical Study Manager who is keen to work in both science and operations. Early phase project management expeirence would be preferable.

    This is a permanent and full-time role. The role would be home-based initially with some travel to the office in the long-run. They offer an excellent salary + bonus.

    Skills Alliance are the preferred supplier for this role. Please contact Mark Anderson for more details – +44 207 220 6209 or click apply now.

  • Clinical Operations

    £50000 - £60000 per annum, excellent package
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    A rare opportunity to join a fast growing Advanced Therapies focused Biotech. This is a permanent Clinical Trial Manager or Clinical Study Manager role based in the London area.

    This exciting and innovative Biotech company are at early stages with trials working in advanced therapies. They are expanding at present and will offer great long-term prospects. The company are looking for an experienced Junior Study Manager or Clinical Trial Manager, this would be working on interesting studies from phase I-III. They require a clinical trial management experience, ideally experience in early phase, complex TAs and experience of working with sites. They have multiple programs ongoing and have a global presence.

    This is a full-time and permanent position. It is office-based in the London area with flexibility to work from home (home-based during the pandemic). They offer an excellent salary and package around GBP 50-60K depending on experience + bonus + extensive benefits.

    Skills Alliance are the preferred supplier for this new CPM / CTM position. For more details please call Mark Anderson on 0207 220 6209 or click apply now.

  • Clinical Operations

    £60000 - £90000 per annum, bonus + shares + benefits
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    I am partnered with an exciting Oncology Biotech in Central London who have a unique model and a strong pipeline.

    This Biotech works specifically in Oncology and have a number of early phase assets, they work in a range of areas within the Oncology field. They have excellent funding and are a very secure organisation despite being relatively small. They plan to remain quite small and outsource the trials to CRO. They have a unique model and are doing exciting work in the cancer field.

    They are recruiting for a Senior Clinical Trial Manager to join the team and need a very experienced and accomplished Project/Study Manager, Ideally with several years working at senior trial management level. Pharma/Biotech experience, significant Oncology experience and early phase (I and II ideally) is required. You are likely to be responsible for several early phase projects. They need someone who autonomous and can work in a small and dynamic team. Protocol writing would be of benefits and experience of working cross-functionally.

    This is a full-time and permanent role, it would be home-based initially and they would want someone in the office several days per week post-COVID. The office is based in Central London. There is an excellent salary and package on offer – £65-90K depending on experience + bonus + benefits + share options.

    Skills Alliance are the exclusive partner for this position, please get in touch with Mark Anderson to find out more on +44 207 220 6209 or APPLY NOW.

  • Clinical Operations

    £60000 - £90000 per annum, Bonus + benefits
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    Great opportunity for an experienced Clinical Project Manager or Study Manager to join a niche Bitoech working in Oncology. The role would be home-based initially with some travel to the office when normality resumes.

    The role is with a niche company who are very innovative and work specifically in Oncology. The company is growing quickly and have exciting early phase programs ongoing. This would be working at the cutting edge of research with a great team who are looking to make a real impact on patients’ lives.

    The position is a wide ranging one given the size of the team. They need an autonomous Senior Clinical Study Manager who is keen to work in both science and operations. Early phase project management expeirence and Oncology trial management is essential for this role.

    This is a permanent and full-time role. The role would be home-based initially with some travel to the London office further down the line. They offer an excellent salary in the region of £65-85K depending on expeirence + bonus + benefits.

    Skills Alliance are the exclusive partner for this role. Please contact Mark Anderson for more details – +44 207 220 6209 or click “APPLY NOW”.

  • Quality

    negotionable
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    Michael Parker at Skills Alliance is currently recruiting several extremely exciting GCP auditor roles. My client are an exciting consultancy that have huge growth plans. The consultancy specialises in QA work solely across all areas of GxP.

    This role is to focus on their huge demand of GCP work their clients need, the clients range from small hyper growth Biotechs to large pharma.

    This is a great opportunity for someone with circa 5 years+ GCP auditing experience to broaden their experience and gain invaluable training and development. You will also get the opportunity to work with UK or global clients as well as get experience in other areas of GxP should you desire.

    The role will cover all areas of external auditing and be completely home based + travel. Below are some of the key responsibilities

    • Plan, conduct, report and follow up contracted audits within agreed budget and timelines
    • Conduct technical peer reviews and provide feedback on client deliverables
    • Assist with the preparation and facilitation of audits and regulatory inspections of clients, and work with responsible parties to prepare Corrective Action and Preventative Action (CAPA) plans as applicable
    • Provide strategic advice to clients on Quality Management System development and change
    • Provide a consultancy service for GCP and/or additional regulations
    • Develop and deliver training programs and/or materials
    • Manage the fulfillment of assigned contracted activities, identifying identify and escalate any potential out-of-scope activities
    • Keep relevant manager(s)/project manager, and the client where applicable, informed of the progress of all assigned contracted activities and any issues that may arise by providing regular updates and maintaining effective communication
    • Foster and maintain good, professional working relationships with clients and identify new business opportunities
    • Assist with the preparation of proposals and presentations to prospective clients

    Skills Required

    • Thorough knowledge of GCP and/or other applicable regulatory requirements
    • Excellent attention to detail, organisation, and prioritisation skills
    • Strong interpersonal skills, verbal and written skills, and the ability to communicate confidently at all levels
    • Self-motivation and ability to function independently and within a team
    • Ability to function calmly under pressure
    • Practical and enquiring approach to problem-solving
    • Dedication to quality and reliability in all aspects of work
    • Responsiveness to customer needs and focus on customer satisfaction

    This role is urgent so please get in touch as soon as possible if this is something you are interested in. Please note this role is only eligible for candidates based in the UK or eligible to work in the UK without sponsorship.

  • Clinical Operations

    €60 - €95 per hour
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    Seeking experienced CER writer to support a Dental implant device (Class IIb), to support a Dental Implants and CAD/CAM-based individualized prosthetics the key responsibilities are as followed:

    – Support in literature review and review of technical documentation
    – Support in leading project meeting related to clinical evaluation
    – Support in writing Clinical Evaluation Reports
    – Ad hoc Support for the line manager for clinical evaluation
    – Affected products: dental implants and their accessories & SaMD (latter is a wish)

    It is a 0.8 – 1 FTE contract starting in April or May and is fully remote, Is an English speaking role.

    The ideal candidates will have over 5 years CER experiance and have written Dental Implants CER. In the past.

  • Clinical Operations

    £60000 - £90000 per annum, bonus + shares + benefits
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    I am partnered with an exciting Oncology Biotech in Central London who have a unique model and a strong pipeline.

    This Biotech works specifically in Oncology and have a number of early phase assets, they work in a range of areas within the Oncology field. They have excellent funding and are a very secure organisation despite being relatively small. They plan to remain quite small and outsource the trials to CRO. They have a unique model and are doing exciting work in the cancer field.

    They are recruiting for a Senior Clinical Trial Manager to join the team and need a very experienced and accomplished Project/Study Manager, Ideally with several years working at senior trial management level. Pharma/Biotech experience, significant Oncology experience and early phase (I and II ideally) is required. You are likely to be responsible for several early phase projects. They need someone who autonomous and can work in a small and dynamic team. Protocol writing would be of benefits and experience of working cross-functionally.

    This is a full-time and permanent role, it would be home-based initially and they would want someone in the office several days per week post-COVID. The office is based in Central London. There is an excellent salary and package on offer – £65-90K depending on experience + bonus + benefits + share options.

    Skills Alliance are the exclusive partner for this position, please get in touch with Mark Anderson to find out more on +44 207 220 6209 or APPLY NOW.

  • Project Management

    £60000 - £70000 per annum, Bonus + benefits
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    Share

    A great opportunity to join a medium-sized CRO with a great culture and low turnover. They are recruiting for PM and Senior PM roles due to organic growth and new studies. *PHARMA EXPERIENCE REQUIRED*

    This company have a great track record and have been very successful during COVID where other CROs have struggled. They are a SME CRO who are dynamic and work in very interesting and complex therapy areas. Studies span phases I-IV and they work in Oncology and Gene Therapy amongst other areas.

    They are recruiting for multiple roles due to new studies coming in and they need an experienced cross-functional PM who has strong budget management experience. It could be working on a range of studies and would be working globally. There are also opportunities to progress quickly.

    This is a permanent and full-time role. They have an office in the South East but everyone is now home-based and this can be a remote role across the UK. They will offer a very good salary – GBP 60-70K + bonus + benefits.

    Skills Alliance are the preferred supplier for this new CPM / CTM position. For more details please call Mark Anderson on 0207 220 6209 or click apply now.

  • Clinical Operations

    £55000 - £65000 per annum, excellent package
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    A rare opportunity to join a growing Gene Therapies focussed Biotech. This is a permanent Clinical Study Manager role based in Central London.

    This exciting and innovative Biotech company are at early stages with trials working in advanced therapies. They are expanding at present and will offer great long-term prospects. The company are looking for an experienced Clinical Study Manager or Clinical Trial Manager, this would be working on complex and fast-paced studies from phase I-III. They require a clinical trial management experience, ideally experience in early phase, complex TAs and interntional trial management expeirence. They have multiple programs ongoing and have a global presence.

    This is a full-time and permanent position. It is office-based in the London with flexibility to work from home (home-based during the pandemic). They offer an excellent salary and package around GBP 55-65K depending on experience + bonus + extensive benefits.

    Skills Alliance are the preferred supplier for this new CPM / CTM position. For more details please call Mark Anderson on 0207 220 6209 or click apply now.

  • Clinical Operations

    £55000 - £65000 per annum, excellent package
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    A rare opportunity to join a growing Gene Therapies focussed Biotech. This is a permanent Senior Clinical Study Manager role based in Central London.

    This exciting and innovative Biotech company are at early stages with trials working in advanced therapies. They are expanding at present and will offer great long-term prospects. The company are looking for a very experienced Clinical Study Manager or Clinical Trial Manager, this would be working on complex and fast-paced studies from phase I-III. They require clinical trial management experience, ideally experience in early phase, complex TAs and interntional trial management expeirence. They have multiple programs ongoing and have a global presence.

    This is a full-time and permanent position. It is office-based in the London with flexibility to work from home (home-based during the pandemic). They offer an excellent salary and package around GBP 70-80K depending on experience + bonus + extensive benefits.

    Skills Alliance are the preferred supplier for this new Senior CPM / Senior CTM position. For more details please call Mark Anderson on 0207 220 6209 or click apply now.

  • Project Management

    £60000 - £75000 per annum, Bonus + benefits
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    Skills Alliance are partnered with a very exciting and growing Biotech at present to hire for an Senior Project Manager (cross-functional) role in London.

    The organisation are going through a period of growth due to their own ongoing trials and a partnership with a leading global Pharma. They work in complex trials across phases I-III and work in areas of unmet medical need to hopefully have a big impact on patients’ lives. We have placed numerous people in their clin ops team in the past three years and have had great feedback. They are UK based but with a global footprint.

    Cross-functional Senior PM for one or two complex trials, with study managers reporting into this position. Matrix management, oversight of budgets and timelines for projects. Previous cross-functional experience required from Biopharma or CRO and working with complex therapy areas.

    This is a permanent and full-time role, based in Central London with flexibility. They will offer an excellent salary and package – £60-75K depending on experience + bonus + benefits.

    Please get in touch with Mark Anderson for more info – 0207 220 6209 or Apply now.

  • Clinical Operations

    £50000 - £65000 per annum, bonus + benefits
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    I am partnered with an exciting Pharma client in the London area to help build out a new team in Oncology.

    This growing Pharmaceutical company works across a range of areas but is investing a lot in Oncology at present. They are a fantastic organisation who offer excellent development opportunities. Given their success in bringing products to market, rate of growth and the new team, this is a rare and exciting proposition. This is working in their Oncology business unit.

    They are recruiting for a Clinical Study Manager to join the team and need an experienced Project/Study Manager with some international trial management expeirence. Pharma/Biotech experience is preferred but they will consider people from CRO and significant Oncology experience is required (CRA or CTM level).

    This is a full-time and permanent role, it would be home-based initially and they would want someone in the office several days per week post-COVID. The office is based in the London area. There is an excellent salary and package on offer – £50-65K depending on experience + bonus + benefits.

    Skills Alliance are the exclusive partner for this position, please get in touch with Mark Anderson to find out more on +44 207 220 6209 or APPLY NOW.

  • Clinical Operations

    £50000 - £65000 per annum, bonus + benefits
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    I am partnered with an exciting Pharma client in the London area to help grow their Infectious Disease team.

    This growing Pharmaceutical company works across a range of areas of unmet medical need including Infectious Disease. They are a fantastic organisation who offer excellent development opportunities. Given their success in bringing products to market and rate of growth, this is a rare and exciting proposition. This is working in their Infectious Disease business unit.

    They are recruiting for a Clinical Study Manager to join the team and need an experienced and accomplished Project/Study Manager with international trial management experience. Pharma/Biotech experience is preferred but they will consider people from CRO. Infectious disease or vaccines experience would be a plus but not required.

    This is a full-time and permanent role, it would be home-based initially and they would want someone in the office several days per week post-COVID. The office is based in the London area. There is an excellent salary and package on offer – £50-65K depending on experience + bonus + benefits.

    Skills Alliance are the exclusive partner for this position, please get in touch with Mark Anderson to find out more on +44 207 220 6209 or APPLY NOW.

  • Clinical Operations

    £60000 - £90000 per annum, bonus + shares + benefits
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    I am partnered with an exciting Pharma client in the London area to help build out a new team in Oncology.

    This Pharma works across a range of areas but is investing a lot in Oncology at present. They are a fantastic organisation who offer excellent development opportunities. Given their success in bringing products to market, rate of growth and the new team, this is a rare and exciting proposition. This is working in their Oncology business unit.

    They are recruiting for a Senior Clinical Study Manager to join the team and need a very experienced and accomplished Oncology Project/Study Manager who would like to take on line management of a small team. Pharma/Biotech experience is preferred and significant Oncology experience is required.

    This is a full-time and permanent role, it would be home-based initially and they would want someone in the office several days per week post-COVID. The office is based in the London area. There is an excellent salary and package on offer – £65-75K depending on experience + bonus + benefits + share options.

    Skills Alliance are the exclusive partner for this position, please get in touch with Mark Anderson to find out more on +44 207 220 6209 or APPLY NOW.

  • Clinical Operations

    $75 - $120 per hour
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    1 FTE Global CPM Consultant – ASAP start – Remote working (less than 10% travel) – Global CRO – W2

    My client are a mid-sized CRO who are looking for an Global CPM Consultant. Rates are hourly and open based on Skillset, the range is not the maxium.

    Primary Purpose
    The Global Clinical Project Manager (CPM) is critical to the successful conduct of Biopharmaceutical-sponsored clinical trials as a matrix leader of the core project team. The CPM is responsible for the successful delivery of a Biopharmaceutical project(s) from the development of the RFP including study budget, proposed staffing and timelines. The CPM will be client-facing and serve as the internal lead of the project through the life cycle of the study, ensuring effective project delivery in agreement with contracted project timeline and budget. The CPM directs project delivery by driving team and financial efficiency, work product quality, and is responsible for client satisfaction through strong relationship management.

    Responsibilities

    • Serves as a primary lead in developing RFPs for biopharma clients, identifying appropriate staff, preparing proposal language, and developing budget and timelines in collaboration with leaders and key subject matter experts (SMEs)
    • Ensures that deliverables for the assigned project/s are completed according to the contract budget, schedule, and quality standards. Projects will be effectively managed in all areas of performance
    • Develops successful working relationships with clients, executive management, and project staff and collaborate to manage project issues, proactively identify and mitigate risks and drive milestone achievement
    • Serves as the primary point of contact for biopharma clients and demonstrate proficiency in knowledge and understanding of client needs
    • Tracks project deliverables against contract using tools. Proactively prepare/present study metrics to maintain transparency for internal/external stakeholders. Monitor trends and drive changes to the plan as needed; identify risks to delivery and agree mitigation plans with the project team to be presented to the client
    • Ensures adherence to quality control expectations and milestone timelines for delivery of contractually required reports and deliverables
    • Oversees all project resources (i.e., budget, personnel, and subcontracts)
    • Identifies and manage changes to scope and requests for out-of-scope activities. Collaborate with Business Development, Contracts Department, and executive management to ensure timely execution of contract amendments/change orders. Prospectively manage client expectations
    • Presents in bid defense meetings in collaboration with Business Development
    • Develops study management plans in collaboration with Clinical Study Manager (CSM)/Clinical Team Lead (CTL), Clinical Research Manager (CRA) and other core team members
    • Identifies and documents lessons learned from study successes and challenges to promote
    • Other duties as assigned on a case by case bases

    Experience

    • Bachelor’s degree in a scientific discipline with a minimum 6 years demonstrating scientific principles appropriate in managing a clinical research portfolio inclusive of 4 or more years in a pharmaceutical and/or CRO setting (CRO prefered), serving in a global Clinical Trial Team Lead or CPM role or equivalent position.
    • Demonstrable track-record of success delivering complex/ high priority clinical trials within agreed time, quality and cost working across multiple therapeutic areas, phases 1-4, in a global capacity
    • Demonstrated experience in developing and fostering strong client and internal relationships
    • Thorough understanding of ICH GCP and all applicable global regulatory regulations and guidelines
    • Skilled in MS Office Suite of products and working knowledge of Clinical Trial Management Systems, electronic Trial Master File, and electronic Data Capture systems and solutions
    • Demonstrated experience in managing diverse staff and leading successful teams with direct and indirect supervision responsibilities

    YOU MUST HAVE THE RIGHT TO WORK IN THE USA FOR THIS ROLE

    If this is a role of intrest please share your CV and I will look to reach out as soon as possible, this is a great opportunity and will not be round for long!

  • Clinical Operations

    £65000 - £75000 per annum, Bonus + benefits
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    Share

    Great opportunity for an experienced Study Manager or Senior Study Manager to join a niche Bitoech working in advanced therapies. The role would be home-based initially with some travel to an office when normality resumes.

    The role is with a niche company who are very innovative and have exciting science. They company are growing quickly and have advanced therapies trials in early stages across several indications. This would be working at the cutting edge of research.

    The position is a wide ranging one given the size of the team. They need an autonomous Senior Clinical Study Manager who is keen to work in both science and operations. Early phase project management expeirence would be preferable and global experience.

    This is a permanent and full-time role. The role would be home-based initially with some travel to the office in the long-run. They offer an excellent salary + bonus.

    Skills Alliance are the preferred supplier for this role. Please contact Mark Anderson for more details – +44 207 220 6209 or click apply now.

  • Pre-Clinical

    £60000 - £65000 per annum, Bonus + benefits
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    A great opportunity to join a medium-sized CRO with a great culture and low turnover. They are recruiting for PM and Senior PM roles due to organic growth and new studies. *PHARMA EXPERIENCE REQUIRED*

    This company have a great track record and have been very successful during COVID where other CROs have struggled. They are a SME CRO who are dynamic and work in very interesting and complex therapy areas. Studies span phases I-IV and they work in Oncology and Gene Therapy amongst other areas.

    They are recruiting for multiple roles due to new studies coming in and they need an experienced cross-functional PM who has budget management experience. It could be working on a range of studies and would be working globally. There are also opportunities to progress quickly.

    This is a permanent and full-time role. They have an office in the South East but everyone is now home-based and this can be a remote role across the UK. They will offer a very good salary – GBP 60-65K + bonus + benefits.

    Skills Alliance are the preferred supplier for this new CPM / CTM position. For more details please call Mark Anderson on 0207 220 6209 or click apply now.

  • Clinical Operations

    £60000 - £70000 per annum, Bonus + benefits
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    Great opportunity for a Study Manager or Senior Study Manager to join a niche Bitoech working in advanced therapies. The role would be home-based initially with some travel to an office when normality resumes!

    The role is with a niche company who are very innovative and have exciting science. They company are growing quickly and have advanced therapies trials in early stages across several indications. This would be working at the cutting edge of research.

    The position is a wide ranging one given the size of the team. They need an autonomous Clinical Study Manager who is keen to work in both science and operations. Early phase project management expeirence would be preferable.

    This is a permanent and full-time role. The role would be home-based initially with some travel to the office in the long-run. They offer an excellent salary + bonus.

    Skills Alliance are the preferred supplier for this role. Please contact Mark Anderson for more details – +44 207 220 6209 or click apply now.

  • Manufacturing

    €135000 - €150000 per annum
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    We are recruiting on behalf of our client, a pharmaceutical company, a Capital Procurement consultant.
    This is a temporary position for 12 month.

    Requirements:
    Understanding CAPEX projects to which procurement support services will be performed, roles
    and responsibilities within the Project Team.
    Understanding procurement tasks and their urgency, prioritisation.
    Alignment on tasks with highest urgency with the Global and Site Procurement
    Representatives and responsible project managers and subject matter experts.
    Continuous cooperation with the relevant business functions and project management
    functions, key stakeholders, early indication of requirements towards
    specifications, bill of quantities, supplier communication, etc.
    Training on local site related requirements with special
    regards to EHS
    Solid and well-working relationship with the engineering and project management
    function, specifications developed in line with the procurement requirements
    enabling competitive selection processes
    Consultant is aware of the EHS and other requirements at site, Request for Proposal (RFP)
    documents, Price Sheets, draft MSAs prepared, RFPs ready to launch
    Reports to the Project Manager and Project sponsors in compliance with the instructions of the Project Manager (weekly and monthly reports).

    Preferred Requirements:

    • minimum 5 years experience with CAPEX in the areas of equipment, engineering design and construction.
    • previous pharmaceutical experience Should you like to receive more information regarding this opportunity, please apply or get in touch with Andreea Coman on 41 (0) 435 088 582, E: andreea.coman@skillsalliance.com
  • Clinical Operations

    £50000 - £60000 per annum, excellent package
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    Share

    A rare opportunity to join a fast growing Advanced Therapies focused Biotech. This is a permanent Clinical Trial Manager or Clinical Study Manager role based in the London area.

    This exciting and innovative Biotech company are at early stages with trials working in advanced therapies. They are expanding at present and will offer great long-term prospects. The company are looking for an experienced Junior Study Manager or Clinical Trial Manager, this would be working on interesting studies from phase I-III. They require a clinical trial management experience, ideally experience in early phase, complex TAs and experience of working with sites. They have multiple programs ongoing and have a global presence.

    This is a full-time and permanent position. It is office-based in the London area with flexibility to work from home (home-based during the pandemic). They offer an excellent salary and package around GBP 50-60K depending on experience + bonus + extensive benefits.

    Skills Alliance are the preferred supplier for this new CPM / CTM position. For more details please call Mark Anderson on 0207 220 6209 or click apply now.

  • Clinical Operations

    £60000 - £90000 per annum, Bonus + benefits
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    Share

    Great opportunity for an experienced Clinical Project Manager or Study Manager to join a niche Bitoech working in Oncology. The role would be home-based initially with some travel to the office when normality resumes.

    The role is with a niche company who are very innovative and work specifically in Oncology. The company is growing quickly and have exciting early phase programs ongoing. This would be working at the cutting edge of research with a great team who are looking to make a real impact on patients’ lives.

    The position is a wide ranging one given the size of the team. They need an autonomous Senior Clinical Study Manager who is keen to work in both science and operations. Early phase project management expeirence and Oncology trial management is essential for this role.

    This is a permanent and full-time role. The role would be home-based initially with some travel to the London office further down the line. They offer an excellent salary in the region of £65-85K depending on expeirence + bonus + benefits.

    Skills Alliance are the exclusive partner for this role. Please contact Mark Anderson for more details – +44 207 220 6209 or click “APPLY NOW”.

  • Manufacturing

    €75 - €80 per hour
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    We are recruiting on behalf of our client, an Engineering Consultancy specialized in C&Q projects in the (bio)phamaceutical industry
    CQV Engineers.
    This is a temporary position for 12+ months.

    Requirements:
    – Strong experience with SAT/Commissioning, IQ and OQ, Design Review (DR) process
    – GMP Risk Assessment (FMEA) experience
    – Identify the appropriate Commissioning and Qualification strategy to apply on specific project and define the list of activities required
    – Review and follow-up technical documentation from the early design phase in order to ensure alignment with GMP and CQV requirements
    – Technical problem solving skills
    – Mechanical Completion procedure and Construction scope of work (Walkdown, system acceptance, punch list and follow up)
    – Schedule preparation and progress review
    – Management and coordination of Contractors and Vendors
    – Final Handover reports to the Client users


    Preferred Requirements:
    – Degree or equivalent in an engineering related discipline
    – 5+ years experience in the pharma and/or biotech industry
    – Fluent in English, any other language an advantage
    – Strong leadership and team player ability, liaising directly with client and other project key functions

    Should you like to receive more information regarding this opportunity, please apply or get in touch with Khaoula Marmada on 41 (0) 435 080 339, E:khaoula.marmada@skillsalliance.com

  • Manufacturing

    €75 - €80 per hour
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    Share

    We are recruiting on behalf of our client, an Engineering Consultancy specialized in C&Q projects in the (bio)phamaceutical industry
    CQV Engineers.
    This is a temporary position for 12+ months.

    Requirements:
    – Strong experience with SAT/Commissioning, IQ and OQ, Design Review (DR) process
    – GMP Risk Assessment (FMEA) experience
    – Identify the appropriate Commissioning and Qualification strategy to apply on specific project and define the list of activities required
    – Review and follow-up technical documentation from the early design phase in order to ensure alignment with GMP and CQV requirements
    – Technical problem solving skills
    – Mechanical Completion procedure and Construction scope of work (Walkdown, system acceptance, punch list and follow up)
    – Schedule preparation and progress review
    – Management and coordination of Contractors and Vendors
    – Final Handover reports to the Client users


    Preferred Requirements:
    – Degree or equivalent in an engineering related discipline
    – 5+ years experience in the pharma and/or biotech industry
    – Fluent in English, any other language an advantage
    – Strong leadership and team player ability, liaising directly with client and other project key functions

    Should you like to receive more information regarding this opportunity, please apply or get in touch with Khaoula Marmada on 41 (0) 435 080 339, E:khaoula.marmada@skillsalliance.com

  • Clinical Operations

    £55000 - £65000 per annum, excellent package
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    Share

    A rare opportunity to join a growing Gene Therapies focussed Biotech. This is a permanent Senior Clinical Study Manager role based in Central London.

    This exciting and innovative Biotech company are at early stages with trials working in advanced therapies. They are expanding at present and will offer great long-term prospects. The company are looking for a very experienced Clinical Study Manager or Clinical Trial Manager, this would be working on complex and fast-paced studies from phase I-III. They require clinical trial management experience, ideally experience in early phase, complex TAs and interntional trial management expeirence. They have multiple programs ongoing and have a global presence.

    This is a full-time and permanent position. It is office-based in the London with flexibility to work from home (home-based during the pandemic). They offer an excellent salary and package around GBP 70-80K depending on experience + bonus + extensive benefits.

    Skills Alliance are the preferred supplier for this new Senior CPM / Senior CTM position. For more details please call Mark Anderson on 0207 220 6209 or click apply now.

  • Project Management

    £60000 - £70000 per annum, Bonus + benefits
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    Share

    A great opportunity to join a medium-sized CRO with a great culture and low turnover. They are recruiting for PM and Senior PM roles due to organic growth and new studies. *PHARMA EXPERIENCE REQUIRED*

    This company have a great track record and have been very successful during COVID where other CROs have struggled. They are a SME CRO who are dynamic and work in very interesting and complex therapy areas. Studies span phases I-IV and they work in Oncology and Gene Therapy amongst other areas.

    They are recruiting for multiple roles due to new studies coming in and they need an experienced cross-functional PM who has strong budget management experience. It could be working on a range of studies and would be working globally. There are also opportunities to progress quickly.

    This is a permanent and full-time role. They have an office in the South East but everyone is now home-based and this can be a remote role across the UK. They will offer a very good salary – GBP 60-70K + bonus + benefits.

    Skills Alliance are the preferred supplier for this new CPM / CTM position. For more details please call Mark Anderson on 0207 220 6209 or click apply now.

  • Clinical Operations

    £55000 - £65000 per annum, excellent package
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    Share

    A rare opportunity to join a growing Gene Therapies focussed Biotech. This is a permanent Clinical Study Manager role based in Central London.

    This exciting and innovative Biotech company are at early stages with trials working in advanced therapies. They are expanding at present and will offer great long-term prospects. The company are looking for an experienced Clinical Study Manager or Clinical Trial Manager, this would be working on complex and fast-paced studies from phase I-III. They require a clinical trial management experience, ideally experience in early phase, complex TAs and interntional trial management expeirence. They have multiple programs ongoing and have a global presence.

    This is a full-time and permanent position. It is office-based in the London with flexibility to work from home (home-based during the pandemic). They offer an excellent salary and package around GBP 55-65K depending on experience + bonus + extensive benefits.

    Skills Alliance are the preferred supplier for this new CPM / CTM position. For more details please call Mark Anderson on 0207 220 6209 or click apply now.

  • Clinical Operations

    £55000 - £65000 per annum, excellent package
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    Share

    A rare opportunity to join a growing Gene Therapies focussed Biotech. This is a permanent Senior Clinical Study Manager role based in Central London.

    This exciting and innovative Biotech company are at early stages with trials working in advanced therapies. They are expanding at present and will offer great long-term prospects. The company are looking for a very experienced Clinical Study Manager or Clinical Trial Manager, this would be working on complex and fast-paced studies from phase I-III. They require clinical trial management experience, ideally experience in early phase, complex TAs and interntional trial management expeirence. They have multiple programs ongoing and have a global presence.

    This is a full-time and permanent position. It is office-based in the London with flexibility to work from home (home-based during the pandemic). They offer an excellent salary and package around GBP 70-80K depending on experience + bonus + extensive benefits.

    Skills Alliance are the preferred supplier for this new Senior CPM / Senior CTM position. For more details please call Mark Anderson on 0207 220 6209 or click apply now.

  • Clinical Operations

    £60000 - £90000 per annum, Bonus + benefits
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    Great opportunity for an experienced Clinical Project Manager or Study Manager to join Global Pharma company working in Oncology. The role would be home-based initially with some travel to the office when normality resumes.

    This is a great opportunity to join a World-class Pharma company with a great reputation and an excellent pipeline in Oncology, they are growing their Oncology division and it is an exciting time to join where you can expect fast progression opportunities. They are very patient centric and are innovative and science focussed.

    The role is a Clinical Project Manager / Clinical Trial Manager position managing studies across Europe and potentially globally. It is specifically in their Oncology division but they have other TAs too. Most of the studies are in phase II and III and they want people with commercial trial management, ideally in Oncology and some international experience.

    This is a permanent and full-time role. The role would be home-based initially with some travel to the London office further down the line. They offer an excellent salary in the region of £55-65K depending on experience + bonus + benefits.

    Skills Alliance are the exclusive partner for this role. Please contact Mark Anderson for more details – +44 207 220 6209 or click “APPLY NOW”.

  • Project Management

    £50000 - £60000 per annum, Excellent package
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    *PHARMA/BIOTECH EXPERIENCE REQUIRED*

    Skills Alliance are partnered to support a growing Biotech to hire for their Project Management team. The company are highly innovative and work in a new and exciting area, they have some exciting partnerships established and are growing rapidly. It is a fanastic time to join and they have a great team in place.

    The role will support the PMO to deliver clinical development projects and work closely with the R&D team. They are looking for someone at PM level who has strong Pharma/Biotech experience – ideally MS Project experience and a PRINCE2 or similar PM qualification would be a plus too. This is a new role due to a lot of expansion and exciting alliances they have running.

    The role is permanent, full-time and home-based initially, they would like someone to go into the Oxford office when normality resumes (with flexibility to WFH). They will offer circa £50-60K + bonus + benefits (may be some flex).

    Skills Alliance are pertnered to support the recruitment for this R&D Proejct Manager role. Please contact Mark Anderson for more info 0207 220 6209 or APPLY NOW.

  • Project Management

    £60000 - £80000 per annum, Excellent package
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    *CRO/PHARMA EXPERIENCE REQUIRED*

    Skills Alliance are retained on a unique opportunity with an innovative vaccine organisation.

    The company specialises in vaccine development to combat epidemic outbreaks such as COVID and Ebola, they are a global partnership of government, civil society, philanthropic and Pharma organisations. They have a unique approach and will have a direct impact on global epidemics in the coming years. With this goal in mind, they are looking to build out the organisation and are looking for high calibre candidates who want to make a difference. They are very well funded and are an employer who is very focused on diversity.

    The Senior Project Manager will facilitate the successful delivery of several vaccine R&D projects associated with the organisation’s mission. Responsible to proactively manage all elements of each project – monitoring, scope, timelines, risk, budget and quality. They require previous cross-functional R&D project management experience, ideally managing projects from pre-clinical to commercialisation (phase I-III). They will consider experienced PMs from Pharma, Biotech or CRO and vaccines experience would be a strong preference.

    This is a full-time and permanent position to be home-based with regular travel to their offices in Central London when normality resumes. They will offer a very competitive salary – circa £60-80K depending on experience + full benefits package.

    Skills Alliance are the exclusive partner for this role, please get in contact with Mark Anderson for more details – +44 207 220 6209.

  • Legal

    £50000 - £60000 per annum, Excellent package
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    *PHARMA/BIOTECH/CRO experience required*

    Skills Alliance are partnered with an excting and fast-growing organisation, they have just secured additional funding and are expanding so it’s a great time to join. They are a niche Biotech firm who work in exciting and cutting edge science and will continue to grow out of their Cambridge offices.

    They are recruiting for a Contracts Manager role which will be drafting, negotiaiting and coordinating a range of contracts, both R&D and commercial. They need an autonomous and self-motivated individual with strong contracts experience in the Pharma sector, this is the only role in contracts in the UK so there is a lot of potential for growth and development.

    The role is permanent and full-time, they would like someone to be in the Cambridge office at least 1-2 days per week and flexibility to work from home the rest of the time. They will offer a very good salary and package and great long-term opportunities.

    Skils Alliance are the preferred partner for this Contracts Manager role, please get in touch with Mark Anderson for more info on 0207 220 6209 or Apply now.

  • Legal

    £50000 - £60000 per annum, Excellent package
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    Share

    *PHARMA/BIOTECH/CRO experience required*

    Skills Alliance are partnered with an exciting and fast-growing organisation, they have just secured additional funding and are expanding so it’s a great time to join. They are a niche Biotech firm who work in exciting and cutting edge science and will continue to grow out of their Cambridge offices.

    They are recruiting for a Contracts Manager role which will be drafting, negotiating and coordinating a range of contracts, both R&D and commercial. They need an autonomous and self-motivated individual with strong contracts experience in the Pharma sector, this is the only role in contracts in the UK so there is a lot of potential for growth and development.

    The role is permanent and full-time, they would like someone to be in the Cambridge office at least 1-2 days per week and flexibility to work from home the rest of the time. They will offer a very good salary and package and great long-term opportunities.

    Skills Alliance are the preferred partner for this Contracts Manager role, please get in touch with Mark Anderson for more info on 0207 220 6209 or Apply now.

  • Clinical Operations

    £60000 - £75000 per annum, Bonus + benefits
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    Skills Alliance are partnered with a very exciting and growing Biotech at present to hire for an Senior Project Manager (cross-functional) role in London.

    The organisation are going through a period of growth due to their own ongoing trials and a partnership with a leading global Pharma. They work in complex trials across phases I-III and work in areas of unmet medical need to hopefully have a big impact on patients’ lives. We have placed numerous people in their clin ops team in the past three years and have had great feedback. They are UK based but with a global footprint.

    Cross-functional Senior PM for one or two complex trials, with study managers reporting into this position. Matrix management, oversight of budgets and timelines for projects. Previous cross-functional experience required from Biopharma or CRO and working with complex therapy areas.

    This is a permanent and full-time role, based in Central London with flexibility. They will offer an excellent salary and package – £60-75K depending on experience + bonus + benefits.

    Please get in touch with Mark Anderson for more info – 0207 220 6209 or Apply now.

  • Clinical Operations

    £50000 - £65000 per annum, bonus + benefits
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    I am partnered with an exciting Pharma client in the London area to help build out a new team in Oncology.

    This growing Pharmaceutical company works across a range of areas but is investing a lot in Oncology at present. They are a fantastic organisation who offer excellent development opportunities. Given their success in bringing products to market, rate of growth and the new team, this is a rare and exciting proposition. This is working in their Oncology business unit.

    They are recruiting for a Clinical Study Manager to join the team and need an experienced Project/Study Manager with some international trial management expeirence. Pharma/Biotech experience is preferred but they will consider people from CRO and significant Oncology experience is required (CRA or CTM level).

    This is a full-time and permanent role, it would be home-based initially and they would want someone in the office several days per week post-COVID. The office is based in the London area. There is an excellent salary and package on offer – £50-65K depending on experience + bonus + benefits.

    Skills Alliance are the exclusive partner for this position, please get in touch with Mark Anderson to find out more on +44 207 220 6209 or APPLY NOW.

  • Clinical Operations

    £50000 - £65000 per annum, bonus + benefits
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    I am partnered with an exciting Pharma client in the London area to help grow their Infectious Disease team.

    This growing Pharmaceutical company works across a range of areas of unmet medical need including Infectious Disease. They are a fantastic organisation who offer excellent development opportunities. Given their success in bringing products to market and rate of growth, this is a rare and exciting proposition. This is working in their Infectious Disease business unit.

    They are recruiting for a Clinical Study Manager to join the team and need an experienced and accomplished Project/Study Manager with international trial management experience. Pharma/Biotech experience is preferred but they will consider people from CRO. Infectious disease or vaccines experience would be a plus but not required.

    This is a full-time and permanent role, it would be home-based initially and they would want someone in the office several days per week post-COVID. The office is based in the London area. There is an excellent salary and package on offer – £50-65K depending on experience + bonus + benefits.

    Skills Alliance are the exclusive partner for this position, please get in touch with Mark Anderson to find out more on +44 207 220 6209 or APPLY NOW.

  • Clinical Operations

    £60000 - £75000 per annum, bonus + shares + benefits
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    I am partnered with an exciting Pharma client in the London area to help build out a new team in Oncology.

    This Pharma works across a range of areas but is investing a lot in Oncology at present. They are a fantastic organisation who offer excellent development opportunities. Given their success in bringing products to market, rate of growth and the new team, this is a rare and exciting proposition. This is working in their Oncology business unit.

    They are recruiting for a Senior Clinical Study Manager to join the team and need a very experienced and accomplished Oncology Project/Study Manager who would like to take on line management of a small team. Pharma/Biotech experience is preferred and significant Oncology experience is required.

    This is a full-time and permanent role, it would be home-based initially and they would want someone in the office several days per week post-COVID. The office is based in the London area. There is an excellent salary and package on offer – £65-75K depending on experience + bonus + benefits + share options.

    Skills Alliance are the exclusive partner for this position, please get in touch with Mark Anderson to find out more on +44 207 220 6209 or APPLY NOW.

  • Pre-Clinical

    £60000 - £65000 per annum, Bonus + benefits
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    A great opportunity to join a medium-sized CRO with a great culture and low turnover. They are recruiting for PM and Senior PM roles due to organic growth and new studies. *PHARMA EXPERIENCE REQUIRED*

    This company have a great track record and have been very successful during COVID where other CROs have struggled. They are a SME CRO who are dynamic and work in very interesting and complex therapy areas. Studies span phases I-IV and they work in Oncology and Gene Therapy amongst other areas.

    They are recruiting for multiple roles due to new studies coming in and they need an experienced cross-functional PM who has budget management experience. It could be working on a range of studies and would be working globally. There are also opportunities to progress quickly.

    This is a permanent and full-time role. They have an office in the South East but everyone is now home-based and this can be a remote role across the UK. They will offer a very good salary – GBP 60-65K + bonus + benefits.

    Skills Alliance are the preferred supplier for this new CPM / CTM position. For more details please call Mark Anderson on 0207 220 6209 or click apply now.

  • Clinical Operations

    £60000 - £70000 per annum, Bonus + benefits
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    Great opportunity for a Study Manager or Senior Study Manager to join a niche Bitoech working in advanced therapies. The role would be home-based initially with some travel to an office when normality resumes!

    The role is with a niche company who are very innovative and have exciting science. They company are growing quickly and have advanced therapies trials in early stages across several indications. This would be working at the cutting edge of research.

    The position is a wide ranging one given the size of the team. They need an autonomous Clinical Study Manager who is keen to work in both science and operations. Early phase project management expeirence would be preferable.

    This is a permanent and full-time role. The role would be home-based initially with some travel to the office in the long-run. They offer an excellent salary + bonus.

    Skills Alliance are the preferred supplier for this role. Please contact Mark Anderson for more details – +44 207 220 6209 or click apply now.

  • Clinical Operations

    £65000 - £75000 per annum, Bonus + benefits
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    Great opportunity for an experienced Study Manager or Senior Study Manager to join a niche Bitoech working in advanced therapies. The role would be home-based initially with some travel to an office when normality resumes.

    The role is with a niche company who are very innovative and have exciting science. They company are growing quickly and have advanced therapies trials in early stages across several indications. This would be working at the cutting edge of research.

    The position is a wide ranging one given the size of the team. They need an autonomous Senior Clinical Study Manager who is keen to work in both science and operations. Early phase project management expeirence would be preferable and global experience.

    This is a permanent and full-time role. The role would be home-based initially with some travel to the office in the long-run. They offer an excellent salary + bonus.

    Skills Alliance are the preferred supplier for this role. Please contact Mark Anderson for more details – +44 207 220 6209 or click apply now.

  • Project Management

    €59.14 - €66.53 per hour
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    We are recruiting on behalf of our client, a leader in the pharmaceutical company a Global Community Engagement Lead, available as soon as possible.
    Ideal Background
    Education:
    Relevant degree, postgraduate and working qualifications preferred in the relevant business or applied behavioral sciences (e.g. Strategy, Business Administration, Leadership Development, Psychology, HRM, MBB, etc).
    Languages:
    Fluent in English
    Experience:
    • Minimum 5 years LD, P&O or large-scale Project Management experience in a highly collaborative and matrixed environment.
    • Strong experience with operational management of complex projects, stakeholder engagement, communication and relationship building skills.
    • Proven analytical and conceptual skills, combined with ability to implement.
    • Experience & comfort with technology for collaboration, including SharePoint (use and administration), MS Teams, Yammer.
    • Ability to work within ambiguity and be flexible and adaptable to changing requirements.
    • Demonstrated systems & strategic thinking, including the ability to look across the system, understand changing dynamics and evolve / develop plans accordingly.
    • Known for strong collaboration and networking with the broader P&O community and other stakeholders.
    • External consulting and/or business leadership experience would be valuable.
    Competency profile
    • Strategic and analytical thinking to understand, diagnose and solve complex business problems using systems lens on issues.
    • Strong relationship management skills with experience in building trust and managing stakeholder relationships in a highly matrixed environment.
    • Ability to adapt and be flexible, comfort with operating in an ambiguous environment and challenging status quo as appropriate. Ability to assess changing situations and adapt accordingly.
    • High level project / program management skills and a high degree of organization and effective self-management.
    • Strong team player with excellent communication skills. Desire and ability to coach and mentor others.
    • Proven business understanding, combined with drive to drive implementation.
    • Role modeling our aspired culture of Curiosity, Inspire and Unboss.
    Specific Professional Competencies
    • Experience in leading large scale, complex LD/ change management interventions or business improvement projects.
    • Experience with and understanding of social leadership and the emerging / changing organizational dynamics.
    • Proven collaborator and communicator.
    • Experience supporting Leaders and Associates in their own personal developmental journeys, understanding of and empathy for the challenges that lie within this.

    This is a 1-year contract.

    Contractor Rate: CHF 59.14 – 66.53 per hour

    If you are interested I would be happy to receive your application at:

    khaoula.marmada@skillsalliance.com

  • Project Management

    £80000 - £90000 per annum, Excellent package
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    Senior Clin Ops role with an Oncology focussed Biopharma in the Oxfordshire area (home-based initially). Working at program level and leading their leading programs.

    This is a rare opportunity to join an exciting and fast-growing Oncology focused Biopharmaceutical company, they have a great pipeline spanning phase I-III and trials being run globally. They are growing and will offer excellent long-term opportunities. We have had excellent feedback from recent placements.

    They are recruiting for a Clinical Program Manager / AD role due to growth and new studies coming up, you would be leading their high profile programs in Oncology and they need a vastly experienced individual, ideally with Oncology trial management experience. They want someone who can work at a senior level and take on a leadership role in the team, line management if desired.

    The role is full-time, permanent and home-based initially, office-based in with flexibility when things return to normal in the Oxfordshire area. They will offer an excellent salary and package – around £80-90K basic salary + bonus + benefits + share options.

    Skills Alliance are the preferred partner for this role. Please get in touch with Mark Anderson for more details – 0207 220 6209.

  • Project Management

    £45000 - £55000 per annum, Excellent package
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    Associate Clinical Study Manager role with an Oncology focussed Biopharma in the Oxfordshire area (home-based initially). Excellent progression opportunities.

    This is a rare opportunity to join an exciting and fast-growing Oncology focused Biopharmaceutical company, they have a great pipeline spanning phase I-III and trials being run globally. They are growing and will offer excellent long-term opportunities. We have had excellent feedback from recent placements.

    They are recruiting for a Junior Clinical Project Manager / Associate Clinical Study Manager role due to growth and new studies coming up, you would be supporting their high profile programs in Oncology and they need an experienced Junior PM or Lead CRA, ideally with some Oncology trial management experience. There will be opportunities to progress and gain international experience.

    The role is full-time, permanent and home-based initially, office-based in with flexibility when things return to normal in the Oxfordshire area. They will offer an excellent salary and package – around £45-55K basic salary + bonus + benefits.

    Skills Alliance are the preferred partner for this role. Please get in touch with Mark Anderson for more details – 0207 220 6209.

  • Clinical Operations

    £50000 - £60000 per annum, excellent package
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    A rare opportunity to join a fast growing Advanced Therapies focused Biotech. This is a permanent Clinical Trial Manager or Clinical Study Manager role based in the London area.

    This exciting and innovative Biotech company are at early stages with trials working in advanced therapies. They are expanding at present and will offer great long-term prospects. The company are looking for an experienced Junior Study Manager or Clinical Trial Manager, this would be working on interesting studies from phase I-III. They require a clinical trial management experience, ideally experience in early phase, complex TAs and experience of working with sites. They have multiple programs ongoing and have a global presence.

    This is a full-time and permanent position. It is office-based in the London area with flexibility to work from home (home-based during the pandemic). They offer an excellent salary and package around GBP 50-60K depending on experience + bonus + extensive benefits.

    Skills Alliance are the preferred supplier for this new CPM / CTM position. For more details please call Mark Anderson on 0207 220 6209 or click apply now.

  • Clinical Operations

    £60000 - £90000 per annum, Bonus + benefits
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    Great opportunity for an experienced Clinical Project Manager or Study Manager to join a niche Bitoech working in Oncology. The role would be home-based initially with some travel to the office when normality resumes.

    The role is with a niche company who are very innovative and work specifically in Oncology. The company is growing quickly and have exciting early phase programs ongoing. This would be working at the cutting edge of research with a great team who are looking to make a real impact on patients’ lives.

    The position is a wide ranging one given the size of the team. They need an autonomous Senior Clinical Study Manager who is keen to work in both science and operations. Early phase project management expeirence and Oncology trial management is essential for this role.

    This is a permanent and full-time role. The role would be home-based initially with some travel to the London office further down the line. They offer an excellent salary in the region of £65-85K depending on expeirence + bonus + benefits.

    Skills Alliance are the exclusive partner for this role. Please contact Mark Anderson for more details – +44 207 220 6209 or click “APPLY NOW”.

  • Tech Ops

    Competitive
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    We are recruiting on behalf of our client, a leader in the pharmaceutical company a AzureAD Security Engineer, available ASAP
    Job purpose:
    • Participate the evaluation, design and development of Active Directory technical requirements, solutions, and implementation roadmap to ensure functional, reliable, secure and cost effective company’s technology environment
    • Ensure continuous improvement within the IAM security architecture and engineering by introducing and implementing emerging security technologies and practices.
    • Provide support and guidance throughout the project lifecycle, including evaluating business requirements and security technologies, planning and implementing technology deployment, working in alignment with security engineering teams, and soliciting feedback from security operations teams and other internal customers
    • Work across business and IT teams to analyze, define and elicit requirements for Active Directory integrations.
    • Provide to global project and operational teams technical support, coordination, expertise and risk analysis on your area of expertise.
    • Effectively liaise with other teams in information security & risk management, infrastructure & architecture management, security engineering as well as business functions to deliver the target technology environment and contribute to IT objectives.
    • Contribute and support efforts for documentation, change management, coordination and action plan tracking for the workstreams assigned.
    • Deploy solutions following enterprise change control in environments as needed per project plan, timeline and scope.
    • Adhere to internal teams processes, SLA and follow the quality standards to meet project compliance requirements.
    • Demonstrated AD engineering and Operations skills, solutions implementation, decision making, incorporating sound security principles and emerging technologies to support and implement enterprise security solutions
    • Work with knowledge engineers/text miners/ontology scientific and technical leads, research scientists, informaticians and management of biomedical research to understand their needs.
    • Design and implement semantic data models, Semantic Web Data Architectures for semantic graph DBs/triplestores.
    • Optimize performances and manage the capacity of different semantic graph DBs/triplestores.
    • Design, implement and operate data flows embedding semantic data.
    • Develop and Optimize SPARQL queries.
    • Provide expert advice for the usage of graphical tools to query triplestores.

    Experience:

    • in depth technical skills on AD/Azure AD
    • 10+ years of relevant working experience in IT Security and IT Architecture
    • 7+ years of experience with Active Directory engineering and infrastructure, with in-depth understand
    • Extensive knowledge in Semantic Data Architecture, Knowledge Representation e.g. RDF, Turtle, Ntriples, OWL, Semantic Data Modeling and reasoning. Expert in SPARQL and optimization of queries. • Deep understanding of semantic web technologies. Recognized expert in Semantic Graph

    Education:
    Advanced degree in Computer Science or recognized working experience in a renowned semantic graph DB lab/group.

    This is a 11 months contract with the possibility to be extended.
    If you are interested I would be happy to receive your application at:

    khaoula.marmada@skillsalliance.com

  • Manufacturing

    COMPETITIVE
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    Skills Alliance are currently partnered with a multinational pharmaceutical company based in Cambridge who is looking to grow their QA team with two additional QA Officers to be focused on QA Operations.

    These positions are an excellent opportunity for someone who is looking to build on their existing QA skills whilst being part of a dynamic team and growing team.

    Requirements:

    • Experience in Batch release, with background in Manufacturing QA and QA Operations
    • Previously worked in QC role and can handle queries from external laboratories.

    Responsibilities will include:

    • Complying with the principles of Good Manufacturing Practice (GMP)
    • Release for sale activity
    • Ensure the QMS is maintained (eg. Deviation / CAPA / Change Control systems)
    • Preparation & Maintenance of Quality/Technical Documents

    These roles are permanent and full-time. Skills Alliance is the preferred supplier for these roles. Please contact Stephanie Khalife for more details on stephanie.khalife@skillsalliance.com or submit your CV for consideration.

  • Clinical Operations

    £50000 - £65000 per annum, bonus + benefits
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    I am partnered with an exciting Pharma client in the London area to help build out a new team in Oncology.

    This growing Pharmaceutical company works across a range of areas but is investing a lot in Oncology at present. They are a fantastic organisation who offer excellent development opportunities. Given their success in bringing products to market, rate of growth and the new team, this is a rare and exciting proposition. This is working in their Oncology business unit.

    They are recruiting for a Clinical Study Manager to join the team and need an experienced Project/Study Manager with some international trial management expeirence. Pharma/Biotech experience is preferred but they will consider people from CRO and significant Oncology experience is required (CRA or CTM level).

    This is a full-time and permanent role, it would be home-based initially and they would want someone in the office several days per week post-COVID. The office is based in the London area. There is an excellent salary and package on offer – £50-65K depending on experience + bonus + benefits.

    Skills Alliance are the exclusive partner for this position, please get in touch with Mark Anderson to find out more on +44 207 220 6209 or APPLY NOW.

  • Project Management

    £60000 - £80000 per annum, Excellent package
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    *CRO/PHARMA EXPERIENCE REQUIRED*

    Skills Alliance are retained on a unique opportunity with an innovative vaccine organisation.

    The company specialises in vaccine development to combat epidemic outbreaks such as COVID and Ebola, they are a global partnership of government, civil society, philanthropic and Pharma organisations. They have a unique approach and will have a direct impact on global epidemics in the coming years. With this goal in mind, they are looking to build out the organisation and are looking for high calibre candidates who want to make a difference. They are very well funded and are an employer who is very focused on diversity.

    The Senior Project Manager will facilitate the successful delivery of several vaccine R&D projects associated with the organisation’s mission. Responsible to proactively manage all elements of each project – monitoring, scope, timelines, risk, budget and quality. They require previous cross-functional R&D project management experience, ideally managing projects from pre-clinical to commercialisation (phase I-III). They will consider experienced PMs from Pharma, Biotech or CRO and vaccines experience would be a strong preference.

    This is a full-time and permanent position to be home-based with regular travel to their offices in Central London when normality resumes. They will offer a very competitive salary – circa £60-80K depending on experience + full benefits package.

    Skills Alliance are the exclusive partner for this role, please get in contact with Mark Anderson for more details – +44 207 220 6209.

  • Project Management

    £60000 - £75000 per annum, Bonus + benefits
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    A great opportunity to join a medium-sized CRO with a great culture and low turnover. They are recruiting for PM and Senior PM roles due to organic growth and new studies. *PHARMA EXPERIENCE REQUIRED*

    This company have a great track record and have been very successful during COVID where other CROs have struggled. They are a SME CRO who are dynamic and work in very interesting and complex therapy areas. Studies span phases I-IV and they work in Oncology and Gene Therapy amongst other areas.

    They are recruiting for multiple roles due to new studies coming in and they need an experienced cross-functional PM who has strong budget management experience. It could be working on a range of studies and would be working globally. There are also opportunities to progress quickly.

    This is a permanent and full-time role. They have an office in the South East but everyone is now home-based and this can be a remote role across the UK. They will offer a very good salary – GBP 60-70K + bonus + benefits.

    Skills Alliance are the preferred supplier for this new CPM / CTM position. For more details please call Mark Anderson on 0207 220 6209 or click apply now.

  • Clinical Operations

    £55000 - £65000 per annum, excellent package
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    A rare opportunity to join a growing Gene Therapies focussed Biotech. This is a permanent Senior Clinical Study Manager role based in Central London.

    This exciting and innovative Biotech company are at early stages with trials working in advanced therapies. They are expanding at present and will offer great long-term prospects. The company are looking for a very experienced Clinical Study Manager or Clinical Trial Manager, this would be working on complex and fast-paced studies from phase I-III. They require clinical trial management experience, ideally experience in early phase, complex TAs and interntional trial management expeirence. They have multiple programs ongoing and have a global presence.

    This is a full-time and permanent position. It is office-based in the London with flexibility to work from home (home-based during the pandemic). They offer an excellent salary and package around GBP 70-80K depending on experience + bonus + extensive benefits.

    Skills Alliance are the preferred supplier for this new Senior CPM / Senior CTM position. For more details please call Mark Anderson on 0207 220 6209 or click apply now.

  • Project Management

    £50000 - £60000 per annum, Excellent package
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    *PHARMA/BIOTECH EXPERIENCE REQUIRED*

    Skills Alliance are partnered to support a growing Biotech to hire for their Project Management team. The company are highly innovative and work in a new and exciting area, they have some exciting partnerships established and are growing rapidly. It is a fanastic time to join and they have a great team in place.

    The role will support the PMO to deliver clinical development projects and work closely with the R&D team. They are looking for someone at PM level who has strong Pharma/Biotech experience – ideally MS Project experience and a PRINCE2 or similar PM qualification would be a plus too. This is a new role due to a lot of expansion and exciting alliances they have running.

    The role is permanent, full-time and home-based initially, they would like someone to go into the Oxford office when normality resumes (with flexibility to WFH). They will offer circa £50-60K + bonus + benefits (may be some flex).

    Skills Alliance are pertnered to support the recruitment for this R&D Proejct Manager role. Please contact Mark Anderson for more info 0207 220 6209 or APPLY NOW.

  • Clinical Operations

    £55000 - £65000 per annum, excellent package
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    A rare opportunity to join a growing Gene Therapies focussed Biotech. This is a permanent Clinical Study Manager role based in Central London.

    This exciting and innovative Biotech company are at early stages with trials working in advanced therapies. They are expanding at present and will offer great long-term prospects. The company are looking for an experienced Clinical Study Manager or Clinical Trial Manager, this would be working on complex and fast-paced studies from phase I-III. They require a clinical trial management experience, ideally experience in early phase, complex TAs and interntional trial management expeirence. They have multiple programs ongoing and have a global presence.

    This is a full-time and permanent position. It is office-based in the London with flexibility to work from home (home-based during the pandemic). They offer an excellent salary and package around GBP 55-65K depending on experience + bonus + extensive benefits.

    Skills Alliance are the preferred supplier for this new CPM / CTM position. For more details please call Mark Anderson on 0207 220 6209 or click apply now.

  • Clinical Operations

    £60000 - £90000 per annum, Bonus + benefits
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    Great opportunity for an experienced Clinical Project Manager or Study Manager to join Global Pharma company working in Oncology. The role would be home-based initially with some travel to the office when normality resumes.

    This is a great opportunity to join a World-class Pharma company with a great reputation and an excellent pipeline in Oncology, they are growing their Oncology division and it is an exciting time to join where you can expect fast progression opportunities. They are very patient centric and are innovative and science focussed.

    The role is a Clinical Project Manager / Clinical Trial Manager position managing studies across Europe and potentially globally. It is specifically in their Oncology division but they have other TAs too. Most of the studies are in phase II and III and they want people with commercial trial management, ideally in Oncology and some international experience.

    This is a permanent and full-time role. The role would be home-based initially with some travel to the London office further down the line. They offer an excellent salary in the region of £55-65K depending on experience + bonus + benefits.

    Skills Alliance are the exclusive partner for this role. Please contact Mark Anderson for more details – +44 207 220 6209 or click “APPLY NOW”.

  • Quality

    negotionable
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    Michael Parker at Skills Alliance is currently recruiting several extremely exciting GCP auditor roles. My client are an exciting consultancy that have huge growth plans. The consultancy specialises in QA work solely across all areas of GxP.

    This role is to focus on their huge demand of GCP work their clients need, the clients range from small hyper growth Biotechs to large pharma.

    This is a great opportunity for someone with circa 5 years+ GCP auditing experience to broaden their experience and gain invaluable training and development. You will also get the opportunity to work with UK or global clients as well as get experience in other areas of GxP should you desire.

    The role will cover all areas of external auditing and be completely home based + travel. Below are some of the key responsibilities

    • Plan, conduct, report and follow up contracted audits within agreed budget and timelines
    • Conduct technical peer reviews and provide feedback on client deliverables
    • Assist with the preparation and facilitation of audits and regulatory inspections of clients, and work with responsible parties to prepare Corrective Action and Preventative Action (CAPA) plans as applicable
    • Provide strategic advice to clients on Quality Management System development and change
    • Provide a consultancy service for GCP and/or additional regulations
    • Develop and deliver training programs and/or materials
    • Manage the fulfillment of assigned contracted activities, identifying identify and escalate any potential out-of-scope activities
    • Keep relevant manager(s)/project manager, and the client where applicable, informed of the progress of all assigned contracted activities and any issues that may arise by providing regular updates and maintaining effective communication
    • Foster and maintain good, professional working relationships with clients and identify new business opportunities
    • Assist with the preparation of proposals and presentations to prospective clients

    Skills Required

    • Thorough knowledge of GCP and/or other applicable regulatory requirements
    • Excellent attention to detail, organisation, and prioritisation skills
    • Strong interpersonal skills, verbal and written skills, and the ability to communicate confidently at all levels
    • Self-motivation and ability to function independently and within a team
    • Ability to function calmly under pressure
    • Practical and enquiring approach to problem-solving
    • Dedication to quality and reliability in all aspects of work
    • Responsiveness to customer needs and focus on customer satisfaction

    This role is urgent so please get in touch as soon as possible if this is something you are interested in. Please note this role is only eligible for candidates based in the UK or eligible to work in the UK without sponsorship.

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    Michael Parker at Skills Alliance has exclusively partnered on a retained search for an with an exciting Cell Gene Therapy company. They are looking for an experience regulatory candidate who specifically has experience working with the FDA. The role can sit at either AD or Director level and will be the most senior Regulatory person in the business.

    The client are doing extremely well with a healthy pipeline as they approach late phase clinical they are now looking to bring RA in house. They have a head office in Oxford, UK and a new office in Boston MA. They are happy for this person to be based remotely with trips into to either office.

    For this role it is imperative that you have lead and submitted applications for the FDA.

    I have provided further details below for this particular role below. However if you are interested in going through the 4full details on this role or one of the 3 other senior Reg roles we currently have please get in touch as soon as possible.

    Please note this role is also only available for candidates who are eligible to work and live in the UK or USA without sponsorship or a visaJob description

    • Primary responsibilities include planning, preparation, submission and maintenance of IND’s and CTA’s in USA and EU, and liaison role with CRO’s
    • Regulatory affairs activities and deliverables include providing strategic, technical and regulatory input for medical products (drugs products and medical devices), CMC for the development of human medicinal products, GMP manufacturing of both drug products and devices, clinical development, regulatory filings.
    • Technical authorship of Clinical Trial Applications, INDs, Marketing Authorisation Applications, New Drug Applications, Scientific Advice and Meeting Briefing Documents
    • Planning and execution of launch and commercialization activities and support for commercial/marketing, market access, PV, compliance and quality/supply chain throughout the product lifecycle
    • Filing and review of US-FDA/EMA/NCA applications for the New drug products and Medical devices
    • Communicate and liaise with regulatory agencies as needed to support the development of the regulatory submissions and Educate internal stakeholders on current regulatory trends and expectations.
    • Collaborate across functions and find the balance between quality/regulatory standards and start-up agility

    Education and Technical Experience

    • MS, PhD in Pharmacy, Chemistry, Biochemistry, or Pharmacology, or a related scientific discipline or equivalent combined education and experience.
    • In-depth knowledge of 21 CFR 210/211, Eudralex EU GMP, 21 CFR part 820, 21 CFR part 312, 21 CFR part 316, ISO 13485, MDR and other international regulations and standards for both drug products and medical devices.
    • Experience in preparation of IND and CTA applications for drug products required, preferably experience weighted toward US-FDA. Experience in writing Technical Files and 510(k) or PMA applications for medical devices is an advantage.
    • Clinical development and/or pharmaceutical industries experience required.
    • Approximately ten years of regulatory affairs experience with both drug products and medical devices, with experience in ophthalmology as a preference. Experience in clinical study design and with combination drug-device products is an advantage.
    • Experience in interactions with health authorities and hands-on experience managing regulatory programs from product development through clinical development and the approval process.
    • Experience in regulatory support of drug development, including clinical product development: chemistry, manufacturing, and controls development, non-clinical development, or clinical development. Preference for candidates with significant experience in drug development for the United States and Europe. Exposure to development of new chemical entities is an advantage.
    • Preferably, experience in medical product start-up/fast growth company or similar working environment. Willing to go the extra mile. RAC/TOPRA accreditation is an advantage.


    Please get in touch as soon as possible for full details.

  • Regulatory

    Competitive
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    Michael Parker at Skills Alliance has exclusively partnered on a retained search for an with an exciting Cell Gene Therapy company. They are looking for an experience regulatory candidate who specifically has experience working with the FDA. The role can sit at either AD or Director level and will be the most senior Regulatory person in the business.

    The client are doing extremely well with a healthy pipeline as they approach late phase clinical they are now looking to bring RA in house. They have a head office in Oxford, UK and a new office in Boston MA. They are happy for this person to be based remotely with trips into to either office.

    For this role it is imperative that you have lead and submitted applications for the FDA.

    I have provided further details below for this particular role below. However if you are interested in going through the 4full details on this role or one of the 3 other senior Reg roles we currently have please get in touch as soon as possible.

    Please note this role is also only available for candidates who are eligible to work and live in the UK or USA without sponsorship or a visaJob description

    • Primary responsibilities include planning, preparation, submission and maintenance of IND’s and CTA’s in USA and EU, and liaison role with CRO’s
    • Regulatory affairs activities and deliverables include providing strategic, technical and regulatory input for medical products (drugs products and medical devices), CMC for the development of human medicinal products, GMP manufacturing of both drug products and devices, clinical development, regulatory filings.
    • Technical authorship of Clinical Trial Applications, INDs, Marketing Authorisation Applications, New Drug Applications, Scientific Advice and Meeting Briefing Documents
    • Planning and execution of launch and commercialization activities and support for commercial/marketing, market access, PV, compliance and quality/supply chain throughout the product lifecycle
    • Filing and review of US-FDA/EMA/NCA applications for the New drug products and Medical devices
    • Communicate and liaise with regulatory agencies as needed to support the development of the regulatory submissions and Educate internal stakeholders on current regulatory trends and expectations.
    • Collaborate across functions and find the balance between quality/regulatory standards and start-up agility

    Education and Technical Experience

    • MS, PhD in Pharmacy, Chemistry, Biochemistry, or Pharmacology, or a related scientific discipline or equivalent combined education and experience.
    • In-depth knowledge of 21 CFR 210/211, Eudralex EU GMP, 21 CFR part 820, 21 CFR part 312, 21 CFR part 316, ISO 13485, MDR and other international regulations and standards for both drug products and medical devices.
    • Experience in preparation of IND and CTA applications for drug products required, preferably experience weighted toward US-FDA. Experience in writing Technical Files and 510(k) or PMA applications for medical devices is an advantage.
    • Clinical development and/or pharmaceutical industries experience required.
    • Approximately ten years of regulatory affairs experience with both drug products and medical devices, with experience in ophthalmology as a preference. Experience in clinical study design and with combination drug-device products is an advantage.
    • Experience in interactions with health authorities and hands-on experience managing regulatory programs from product development through clinical development and the approval process.
    • Experience in regulatory support of drug development, including clinical product development: chemistry, manufacturing, and controls development, non-clinical development, or clinical development. Preference for candidates with significant experience in drug development for the United States and Europe. Exposure to development of new chemical entities is an advantage.
    • Preferably, experience in medical product start-up/fast growth company or similar working environment. Willing to go the extra mile. RAC/TOPRA accreditation is an advantage.


    Please get in touch as soon as possible for full details.

  • Regulatory

    Competitive
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    Michael Parker at Skills Alliance has partnered with an exciting and innovative Cell Gene therapy company. The client have recently gone through several successful fundraising so are now looking to hire several QA roles. Please note this is one of several roles so if you are interested get in contact as soon as possible.

    JOB DESCRIPTION:

    The Quality Assurance Officer will be critical in supporting the Quality Management System. This role will be responsible of providing day-to-day assistance for QA activities, including the effective execution of overall QMS, with focus in supporting Clinical QA.

    Job Responsibilities

    • Maintain and monitor QMS performance, including the compilation of quality metrics in support of the QMS Annual report and management review (deviations, CAPAs, training, Periodic Review, etc).
    • Manage the QMS documentation structure and assure all procedures, work instructions, and forms (including revision levels) are in compliance
    • Support and monitor GxP training by recording and archiving of training records in a timely manner. Maintain the training database. Create and assign training curricula to staff. Generate training reports and discuss with management any potential areas of improvement. Monitor the timely completion of training assignments.
    • Assist with document and record management activities including tracking and review of Quality documents, archiving, and periodic review. Ensure that the review of controlled documents occurs in a timely manner. Serve as liaison across functions to ensure documents incorporate input from the key stakeholders.
    • Support activities relating to deviations and CAPAs with focus on clinical deviation investigations.
    • Engage and work with others to further configure the electronic QMS system, deploy functional enhancements, and correct configuration issues.
    • Develop and maintain organized records that demonstrate compliance to all company processes, regulations, and the company’s QMS.
    • Conduct analyses of data pertaining to key performance indicators (KPIs), quality metrics..
    • Additional duties as assigned.



    Please get touch as soon as possible if you are interested in finding out more about this role, or some of the other roles that we are currently recruiting in the QA department at the moment.

  • Quality

    Competitive
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    Michel Parker at Skills Alliance is currently recruiting a Head of Quality to work for a new and exciting CRO.

    Responsibilities:
    Directs and leads entire QA program in both US and UK locations.

    • Partners with internal and global external clients to manage a best-in-class GCP Quality Assurance (QA) program which enhances the organization’s capabilities and continued growth.
    • Oversees Quality Assurance team by providing guidance and direction to ensure departmental and client/project goals are met; coaches and develops team members.
    • Manages the global GXP QA process and implements QA initiatives/audit programs, including IT QA projects, all of which lead to continuous improvement.
    • Manages the corrective/preventive action plan (CAPA) process to ensure timely implementation of CAPAs, and escalation, as applicable.
    • Conducts GXP audits of company systems, CRAs, clinical sites, external vendors and GMP audits as needed and ensures appropriate follow-up.
    • Develops and leads audit /inspection readiness activities to ensure staff members are prepared to proactively participate in regulatory inspections and audits, and appropriately address outcomes.
    • Assists in facilitation of client audits and regulatory inspections.
    • Oversees quality system which provides guidance, tracking, and metrics of compliance.
    • Mitigate risks by developing solutions to everyday problems relating to current projects as well as providing guidance and long-range solutions as a means of preventing repeat and/or additional problems.
    • Oversees Theradex SOP development process and compliance.
    • Leads all training programs & initiatives while also administrating electronic training database


    Qualifications:

    • Minimum of a BA/BS in Science required.
    • Advanced degree preferred.Prior experience leading GCP Quality Assurance programs and interfacing with the FDA & EMA.
    • International and oncology experience preferred.
    • Management experience, 7+ years in a CRO/pharmaceutical environment, is required.
    • Thorough knowledge and experience with GXP quality assurance initiatives / programs and regulatory requirements.Strategic and critical thinking skills.
    • Strong leadership and communications skills (verbal and written).Excellent interpersonal skills.Highly organised and result orientated.
    • Effective ability to meet short- and long-term goals.
    • Effective ability to anticipate challenges and to develop and implement solutions.
    • Effective knowledge of MS Office computer skills.
    • The ability and willingness to travel as required in the US and Internationally.
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    Michael Parker at Skills Alliance has partnered with an exciting and innovative Cell Gene therapy company. The client have recently gone through several successful fundraising so are now looking to hire several QA roles. This is for a QMS lead at AD level.
    This position will be responsible for managing, administering and monitoring of Quality Management Systems, specifically the Deviation, Audit, Change Control, Vendor Management and CAPA processes. Enhancement of existing procedures, and creation of new best practices will be a critical component of this role.

    Essential Duties

    • Leading and managing QA’s day-to-day activities in support of QMS with focus on the development, deployment, and management of the eQMS system (e.g., Deviations, CAPAs, Auditing, Change and Vendor Management, etc).
    • Lead the QMS Program, specifically the deviation, CAPA, Audits, Vendor Mgt & change control programs.
    • Develop, improve, and administer the QMS Program.
    • Serve as Quality Events Champion. Monitor Quality Events, Deviations and CAPAs. Track and trend these and monitor CAPA effectiveness.
    • Provide subject matter expertise to improve the QMS.
    • Develop and improve Quality department procedures.
    • Generate and monitor quality metrics to ensure on-time record closure and identify corrective actions. Development, implement, and report applicable quality metrics and KPIs.
    • Develop and present QMS metrics to management, as required.
    • Create best practices for authoring technical investigations, root cause analysis tools, and corrective and preventive actions.
    • Deliver training to the whole organization on QMS topics, as needed.
    • Support internal and external audits related to the QMS. Managing the internal audit schedule. This includes generation of reports and CAPAs and following up on all action items to ensure their timely closure.
    • Monitor and schedule vendor qualifications. Ensure these are conducted according to schedule.
    • Support the change management program by help drive change controls to completion.


    Education, Experience and Personal Qualities Requirements

    • Meet the minimum required years of experience in a related Biopharmaceutical QMS role
      • Sr Manager – 10 years
      • Assoc Director – 15 years
    • Experience in Biopharmaceutical QA and/or Quality System improvement roles is preferred.
    • A BA or BS is preferred though long-time experience in QA may be acceptable
    • Gene therapy experience is a plus
    • Strong organizational skills and attention to detail
    • Strong interpersonal and communication skills
    • Computer skills and previous experience with eQMS
    • Ability to provide subject matter expertise regarding QMS implementation and administration
    • Past experience managing complex projects is required.
    • Ability to identify areas of improvement and provide solutions. Excellent technical writing and problem-solving skills.
    • Ability to work effectively at a fast-paced environment with cross functional departments. This role requires the incumbent to be able to quickly adapt to changing priorities.
    • Ability to work independently and with minimal supervision is required.
    • Some travel may be required (~20%)
    • MS Office proficiency
    • Project Management experience

    Preferred Qualifications

    • Experience with Gene Therapy / Cell Therapy products
    • Previous experience with MasterControl
    • Entrepreneurial and results driven


    Please note this is one of several roles Skills Alliance are currently recruiting, so if you are interested get in contact as soon as possible.

  • Clinical Operations

    £60000 - £75000 per annum, Bonus + benefits
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    Skills Alliance are partnered with a very exciting and growing Biotech at present to hire for an Senior Project Manager (cross-functional) role in London.

    The organisation are going through a period of growth due to their own ongoing trials and a partnership with a leading global Pharma. They work in complex trials across phases I-III and work in areas of unmet medical need to hopefully have a big impact on patients’ lives. We have placed numerous people in their clin ops team in the past three years and have had great feedback. They are UK based but with a global footprint.

    Cross-functional Senior PM for one or two complex trials, with study managers reporting into this position. Matrix management, oversight of budgets and timelines for projects. Previous cross-functional experience required from Biopharma or CRO and working with complex therapy areas.

    This is a permanent and full-time role, based in Central London with flexibility. They will offer an excellent salary and package – £60-75K depending on experience + bonus + benefits.

    Please get in touch with Mark Anderson for more info – 0207 220 6209 or Apply now.

  • Clinical Development

    £55000 - £75000 per annum, car allowance + bonus + benefits
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    I am partnered with a leading global Pharmaceutical company to hire multiple Clinical Scientist roles at a senior level – Senior Manager / Associate Director level.

    This is a great opportunity to join a World-class Pharma company in their growing team which would be working gloablly. There are excellent development opportunities and the company is well established and has a great reputation.

    They need someone with excellent experience of writing clinical development plans and protocols. The role(s) are at the equivalent to Senior Manager / AD. The next step up would be Director level. They need significant clinical scientist experience but are flexible on background. A Masters or PhD would be preferred.

    The roles would be home-based initially and office-based with flexibility later in the year. The office is based in the Surrey/London area. They will offer an excellent salary – £55-75K depending on level + car allowance + bonus + benefits.

    Skills Alliance are the exclusive partner for these roles. Please get in touch with Mark Anderson for more details +44 207 220 6209 or APPLY NOW.

  • Clinical Development

    £55000 - £75000 per annum, car allowance + bonus + benefits
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    I am partnered with a leading global Pharmaceutical company to hire multiple Clinical Scientist roles at a senior level – Senior Manager / Associate Director level.

    This is a great opportunity to join a World-class Pharma company in their growing team which would be working globally. There are excellent development opportunities and the company is well established and has a great reputation.

    They need someone with excellent experience of writing clinical development plans and protocols. The role(s) are at the equivalent to Senior Manager / AD. The next step up would be Director level. They need significant clinical scientist experience but are flexible on background. A Masters or PhD would be preferred.

    The roles would be home-based initially and office-based with flexibility later in the year. The office is based in the Surrey/London area. They will offer an excellent salary – £55-75K depending on level + car allowance + bonus + benefits.

    Skills Alliance are the exclusive partner for these roles. Please get in touch with Mark Anderson for more details +44 207 220 6209 or APPLY NOW.

  • Clinical Development

    £55000 - £75000 per annum, car allowance + bonus + benefits
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    I am partnered with a leading global Pharmaceutical company to hire multiple Clinical Scientist roles at a senior level – Senior Manager / Associate Director level.

    This is a great opportunity to join a World-class Pharma company in their growing team which would be working globally. There are excellent development opportunities and the company is well established and has a great reputation.

    They need someone with excellent experience of writing clinical development plans and protocols. The role(s) are at the equivalent to Senior Manager / AD. The next step up would be Director level. They need significant clinical scientist experience but are flexible on background. A Masters or PhD would be preferred.

    The roles would be home-based initially and office-based with flexibility later in the year. The office is based in the Surrey/London area. They will offer an excellent salary – £55-75K depending on level + car allowance + bonus + benefits.

    Skills Alliance are the exclusive partner for these roles. Please get in touch with Mark Anderson for more details +44 207 220 6209 or APPLY NOW.

  • Clinical Operations

    £65000 - £75000 per annum, Bonus + benefits
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    Great opportunity for an experienced Study Manager or Senior Study Manager to join a niche Bitoech working in advanced therapies. The role would be home-based initially with some travel to an office when normality resumes.

    The role is with a niche company who are very innovative and have exciting science. They company are growing quickly and have advanced therapies trials in early stages across several indications. This would be working at the cutting edge of research.

    The position is a wide ranging one given the size of the team. They need an autonomous Senior Clinical Study Manager who is keen to work in both science and operations. Early phase project management expeirence would be preferable and global experience.

    This is a permanent and full-time role. The role would be home-based initially with some travel to the office in the long-run. They offer an excellent salary + bonus.

    Skills Alliance are the preferred supplier for this role. Please contact Mark Anderson for more details – +44 207 220 6209 or click apply now.

  • Clinical Operations

    £60000 - £70000 per annum, Bonus + benefits
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    Great opportunity for a Study Manager or Senior Study Manager to join a niche Bitoech working in advanced therapies. The role would be home-based initially with some travel to an office when normality resumes!

    The role is with a niche company who are very innovative and have exciting science. They company are growing quickly and have advanced therapies trials in early stages across several indications. This would be working at the cutting edge of research.

    The position is a wide ranging one given the size of the team. They need an autonomous Clinical Study Manager who is keen to work in both science and operations. Early phase project management expeirence would be preferable.

    This is a permanent and full-time role. The role would be home-based initially with some travel to the office in the long-run. They offer an excellent salary + bonus.

    Skills Alliance are the preferred supplier for this role. Please contact Mark Anderson for more details – +44 207 220 6209 or click apply now.

  • Project Management

    £45000 - £55000 per annum, Excellent package
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    Associate Clinical Study Manager role with an Oncology focussed Biopharma in the Oxfordshire area (home-based initially). Excellent progression opportunities.

    This is a rare opportunity to join an exciting and fast-growing Oncology focused Biopharmaceutical company, they have a great pipeline spanning phase I-III and trials being run globally. They are growing and will offer excellent long-term opportunities. We have had excellent feedback from recent placements.

    They are recruiting for a Junior Clinical Project Manager / Associate Clinical Study Manager role due to growth and new studies coming up, you would be supporting their high profile programs in Oncology and they need an experienced Junior PM or Lead CRA, ideally with some Oncology trial management experience. There will be opportunities to progress and gain international experience.

    The role is full-time, permanent and home-based initially, office-based in with flexibility when things return to normal in the Oxfordshire area. They will offer an excellent salary and package – around £45-55K basic salary + bonus + benefits.

    Skills Alliance are the preferred partner for this role. Please get in touch with Mark Anderson for more details – 0207 220 6209.

  • Pre-Clinical

    £80000 - £90000 per annum, Excellent package
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    Senior Clin Ops role with an Oncology focussed Biopharma in the Oxfordshire area (home-based initially). Working at program level and leading their leading programs.

    This is a rare opportunity to join an exciting and fast-growing Oncology focused Biopharmaceutical company, they have a great pipeline spanning phase I-III and trials being run globally. They are growing and will offer excellent long-term opportunities. We have had excellent feedback from recent placements.

    They are recruiting for a Clinical Program Manager / AD role due to growth and new studies coming up, you would be leading their high profile programs in Oncology and they need a vastly experienced individual, ideally with Oncology trial management experience. They want someone who can work at a senior level and take on a leadership role in the team, line management if desired.

    The role is full-time, permanent and home-based initially, office-based in with flexibility when things return to normal in the Oxfordshire area. They will offer an excellent salary and package – around £80-90K basic salary + bonus + benefits + share options.

    Skills Alliance are the preferred partner for this role. Please get in touch with Mark Anderson for more details – 0207 220 6209.

  • Pre-Clinical

    £80000 - £90000 per annum, Excellent package
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    Associate Director, Clinical Operations role with an Oncology focussed Biopharma in the Oxfordshire area (home-based initially). Working at program level and leading their leading high profile programs.

    This is a rare opportunity to join an exciting and fast-growing Oncology focused Biopharmaceutical company, they have a great pipeline spanning phase I-III and trials being run globally. They are growing and will offer excellent long-term opportunities. We have had excellent feedback from recent placements.

    They are recruiting for a Clinical Program Manager / AD role due to growth and new studies coming up, you would be leading their high profile programs in Oncology and they need a vastly experienced individual, ideally with Oncology trial management experience. They want someone who can work at a senior level and take on a leadership role in the team, line management if desired.

    The role is full-time, permanent and home-based initially, office-based in with flexibility when things return to normal in the Oxfordshire area. They will offer an excellent salary and package – around £80-90K basic salary + bonus + benefits + share options.

    Skills Alliance are the preferred partner for this role. Please get in touch with Mark Anderson for more details – 0207 220 6209.

  • Clinical Development

    £55000 - £75000 per annum, car allowance + bonus + benefits
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    I am partnered with a leading global Pharmaceutical company to hire multiple Clinical Scientist roles at Principal level – equivalent to Senior Manager / Associate Director.

    This is a great opportunity to join a World-class Pharma company in their growing team which would be working globally. There are excellent development opportunities and the company is well established and has a great reputation.

    They need someone with excellent experience of writing clinical development plans and protocols. The role(s) are at the equivalent to Senior Manager / AD. The next step up would be Director level. They need significant clinical scientist experience but are flexible on background. A Masters or PhD would be preferred.

    The roles would be home-based initially and office-based with flexibility later in the year. The office is based in the Surrey/London area. They will offer an excellent salary – £55-75K depending on level + car allowance + bonus + benefits.

    Skills Alliance are the exclusive partner for these roles. Please get in touch with Mark Anderson for more details +44 207 220 6209 or APPLY NOW.

  • Procurement

    $200000 - $240000 per annum
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    Are you an experienced, environmentally-conscious procurement leader? Are you seeking a new opportunity within a forward-thinking, innovative global organization that are striving to make a difference? If so, Skills Alliance has an exciting opportunity for you!

    Our client are an multi-national Pharmaceutical business. Through exponential growth, they have implemented a truly best-in-class procurement function in the US, with significant ambitions to continuously improve operations on a number of fronts. A key component of this improvement initiative involves their carbon footprint – Across their own internal operations and that of their key partners.

    They are now seeking to appoint a new Director for Supplier Sustainability full-time within their organization to drive forward and meet ambitious targets for reducing emissions, as outlined by the company CEO. This exciting role will see you partnering stakeholders across direct & indirect category procurement, internal leadership across a wide range of operations, as well as externally with existing supplier partners across the US, EMEA and APAC.

    Required experience:

    • A proven track record in global procurement leadership.
    • Previous experience implementing sustainable/environmentally-conscious procurement practices.
    • A real passion for driving ethical, sustainable ways of working.
    • Procurement/strategic sourcing experience across wide range of categories.
    • Ideally you will have previous experience working in the life sciences industry, however as long as your experience includes global companies and demonstrates implementing sustainable practice this is the primary criteria.
    • You will need to be a current US citizen in order to be considered.
    • Ideally based full-time in Massachusetts, however any candidates based elsewhere in the US that are willing to travel occasionally, will also be considered.

    Interested? Please apply and Jim Bellicoso will be in touch to discuss and outline next steps. We are looking to move forwards with this quickly, with the client seeking to appoint the role in Q2/Q3 this year!

  • Clinical Operations

    £60000 - £90000 per annum, Bonus + benefits
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    Great opportunity for an experienced Clinical Project Manager or Study Manager to join a niche Bitoech working in Oncology. The role would be home-based initially with some travel to the office when normality resumes.

    The role is with a niche company who are very innovative and work specifically in Oncology. The company is growing quickly and have exciting early phase programs ongoing. This would be working at the cutting edge of research with a great team who are looking to make a real impact on patients’ lives.

    The position is a wide ranging one given the size of the team. They need an autonomous Senior Clinical Study Manager who is keen to work in both science and operations. Early phase project management expeirence and Oncology trial management is essential for this role.

    This is a permanent and full-time role. The role would be home-based initially with some travel to the London office further down the line. They offer an excellent salary in the region of £65-85K depending on expeirence + bonus + benefits.

    Skills Alliance are the exclusive partner for this role. Please contact Mark Anderson for more details – +44 207 220 6209 or click “APPLY NOW”.

  • Clinical Operations

    £500 - £650 per day
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    Freelance Assignment – 2 – 3 days a week – Outside IR35 – COVID Distrabution PM – REMOTE

    Want to support a COVID-19 Vaccine Task-force? The global Distribution team are in need of support. The successful candidate will work with the SCO Strategic Initiatives Lead on one or more strategic initiatives to support the effective working of the cross-partner technical teams for each initiative to move ahead with pace.

    On offer is a unique contract that anyone within the EMEA are able to apply. For UK based consultants the role will be outside of IR35. The workload will be flexiable usally avaerging at 2.5 – 3 days a week on a remote basis.

    Objectives and deliverables

    The support will consist of:

    Programme management and coordination of strategic initiatives:

    • Support the set-up of a team, plan, governance, stakeholder engagement plan, and meeting cadence
    • Set up, prepare and debrief meetings
    • Set up and implement key processes to enable the teams for each strategic initiative to work effectively
    • Proactively capture and track actions and decisions
    • Capture, follow up and escalate risks/issues/mitigations

    Knowledge management:

    • Establish a digital collaborationspace for each team
    • Establish a fact base for each topic, incl all relevant materials, and make it accessible to all team members

    Workshop planning and facilitation:

    • Design, plan and deliver cross-partner working sessions and workshops
    • Support the briefing and debriefing of key stakeholders
    • Use innovative and digital facilitation techniques to enhance the quality of remote workshops and effective discussion and decision-making

    Analytics and content development:

    • Provide continuous quantitative data analysis support to the strategic teams to model scenarios and identify options and recommendations.
    • Develop visually strong and impactful content for meetings and briefings, incl the formulation of recommendations in collaboration with the technical team.

    Skills and experience required

    • Strong project management and analytical skills, with min 3 – 5 years’ experience, preferably with a top tier Consulting company,
    • Impeccable stakeholder engagement experience and ability to engage with stakeholders comfortably and professionally at all levels,
    • Experience in setting plans and executing upon them,
    • Experience in setting up and managing governance models in complex organizations and with complex stakeholders,
    • Experience in developing and evaluating quantitative models, and developing meaningful insights and recommendations based on the data,
    • Advanced ppt skills and ability to draft impactful materials for senior stakeholders with quick turn around,
    • Ability to work in fast-paced, high pressure environment with senior stakeholders across multiple organizations,
    • Calm, professional, proactive demeanor and excellent problem solver.

    For more information please email jack.sinclair@skillsalliance.com

  • Clinical Operations

    £60000 - £70000 per annum
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    (Senior) Project Manager | Homebased

    A leading mid-sized CRO are recruiting for a Cross-functional Project Manager position to be based in Europe.

    This is an amazing opportunity to join an exciting CRO that are expanding out their Clinical Management Team in Europe, will continue to do so over the next few years. There are great opportunities to progress and develop through the company as they continue to grow. They work in a wide range of therapeutic areas such as Oncology and Gene Therapy. This could be working across phases I-III.
    Responsibilities:

    • Acting as a Cross-functional Project manager
    • Create, track and report on project timelines, budgets and deliverables
    • Project Management of global trials
    • Carry out Bid defences and oversight of budgeting and sponsor management

    Requirements:

    • Experience of carrying out Bid defences and Sponsor management
    • Experience as a Project Manager in a CRO

    This Project Manager role is an homeworking position in Poland. It is a permanent role offering around £60-70K + bonus

    Skills Alliance are the preferred supplier for this role. Please contact George Wykes for more details on +44 203 772 8236 or click APPLY NOW.

  • Clinical Operations

    £60000 - £70000 per annum
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    (Senior) Project Manager | Homebased

    A leading mid-sized CRO are recruiting for a Cross-functional Project Manager position to be based in Europe.

    This is an amazing opportunity to join an exciting CRO that are expanding out their Clinical Management Team in Europe, will continue to do so over the next few years. There are great opportunities to progress and develop through the company as they continue to grow. They work in a wide range of therapeutic areas such as Oncology and Gene Therapy. This could be working across phases I-III.
    Responsibilities:

    • Acting as a Cross-functional Project manager
    • Create, track and report on project timelines, budgets and deliverables
    • Project Management of global trials
    • Carry out Bid defences and oversight of budgeting and sponsor management

    Requirements:

    • Experience of carrying out Bid defences and Sponsor management
    • Experience as a Project Manager in a CRO

    This Project Manager role is an homeworking position in Netherlands. It is a permanent role offering around £60-70K + bonus

    Skills Alliance are the preferred supplier for this role. Please contact George Wykes for more details on +44 203 772 8236 or click APPLY NOW.

  • Clinical Operations

    £60000 - £70000 per annum
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    (Senior) Project Manager | Homebased

    A leading mid-sized CRO are recruiting for a Cross-functional Project Manager position to be based in Europe.

    This is an amazing opportunity to join an exciting CRO that are expanding out their Clinical Management Team in Europe, will continue to do so over the next few years. There are great opportunities to progress and develop through the company as they continue to grow. They work in a wide range of therapeutic areas such as Oncology and Gene Therapy. This could be working across phases I-III.
    Responsibilities:

    • Acting as a Cross-functional Project manager
    • Create, track and report on project timelines, budgets and deliverables
    • Project Management of global trials
    • Carry out Bid defences and oversight of budgeting and sponsor management

    Requirements:

    • Experience of carrying out Bid defences and Sponsor management
    • Experience as a Project Manager in a CRO

    This Project Manager role is an homeworking position in Belgium. It is a permanent role offering around £60-70K + bonus

    Skills Alliance are the preferred supplier for this role. Please contact George Wykes for more details on +44 203 772 8236 or click APPLY NOW.

  • Clinical Operations

    £60000 - £70000 per annum
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    (Senior) Project Manager | Homebased

    A leading mid-sized CRO are recruiting for a Cross-functional Project Manager position to be based in Europe.

    This is an amazing opportunity to join an exciting CRO that are expanding out their Clinical Management Team in Europe, will continue to do so over the next few years. There are great opportunities to progress and develop through the company as they continue to grow. They work in a wide range of therapeutic areas such as Oncology and Gene Therapy. This could be working across phases I-III.
    Responsibilities:

    • Acting as a Cross-functional Project manager
    • Create, track and report on project timelines, budgets and deliverables
    • Project Management of global trials
    • Carry out Bid defences and oversight of budgeting and sponsor management

    Requirements:

    • Experience of carrying out Bid defences and Sponsor management
    • Experience as a Project Manager in a CRO

    This Project Manager role is an homeworking position in Spain. It is a permanent role offering around £60-70K + bonus

    Skills Alliance are the preferred supplier for this role. Please contact George Wykes for more details on +44 203 772 8236 or click APPLY NOW.

  • Clinical Operations

    £60000 - £70000 per annum
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    (Senior) Project Manager | Homebased

    A leading mid-sized CRO are recruiting for a Cross-functional Project Manager position to be based in Europe.

    This is an amazing opportunity to join an exciting CRO that are expanding out their Clinical Management Team in Europe, will continue to do so over the next few years. There are great opportunities to progress and develop through the company as they continue to grow. They work in a wide range of therapeutic areas such as Oncology and Gene Therapy. This could be working across phases I-III.
    Responsibilities:

    • Acting as a Cross-functional Project manager
    • Create, track and report on project timelines, budgets and deliverables
    • Project Management of global trials
    • Carry out Bid defences and oversight of budgeting and sponsor management

    Requirements:

    • Experience of carrying out Bid defences and Sponsor management
    • Experience as a Project Manager in a CRO

    This Project Manager role is an homeworking position in Germany. It is a permanent role offering around £60-70K + bonus

    Skills Alliance are the preferred supplier for this role. Please contact George Wykes for more details on +44 203 772 8236 or click APPLY NOW.

  • Clinical Development

    £50000 - £60000 per annum, Excellent package
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    *PHARMA/BIOTECH/CRO experience required*

    Skills Alliance are partnered with an exciting and fast-growing organisation, they have just secured additional funding and are expanding so it’s a great time to join. They are a niche Biotech firm who work in exciting and cutting edge science and will continue to grow out of their Cambridge offices.

    They are recruiting for a Contracts Manager role which will be drafting, negotiating and coordinating a range of contracts, both R&D and commercial. They need an autonomous and self-motivated individual with strong contracts experience in the Pharma sector, this is the only role in contracts in the UK so there is a lot of potential for growth and development. There is the option to grow a small team in future too.

    The role is permanent and full-time, they would like someone to be in the Cambridge office at least 1-2 days per month and flexibility to work from home the rest of the time. They will offer a very good salary and package and great long-term opportunities.

    Skills Alliance are the preferred partner for this Contracts Manager role, please get in touch with Mark Anderson for more info on 0207 220 6209 or Apply now.

  • Project Management

    £60000 - £75000 per annum, Bonus + benefits
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    A great opportunity to join a medium-sized CRO with a great culture and low turnover. They are recruiting for PM and Senior PM roles due to organic growth and new studies. *PHARMA EXPERIENCE REQUIRED*

    This company have a great track record and have been very successful during COVID where other CROs have struggled. They are a SME CRO who are dynamic and work in very interesting and complex therapy areas. Studies span phases I-IV and they work in Oncology and Gene Therapy amongst other areas.

    They are recruiting for multiple roles due to new studies coming in and they need an experienced cross-functional PM who has strong budget management experience. It could be working on a range of studies and would be working globally. There are also opportunities to progress quickly.

    This is a permanent and full-time role. They have an office in the South East but everyone is now home-based and this can be a remote role across the UK. They will offer a very good salary – GBP 60-70K + bonus + benefits.

    Skills Alliance are the preferred supplier for this new CPM / CTM position. For more details please call Mark Anderson on 0207 220 6209 or click apply now.

  • Project Management

    £60000 - £75000 per annum, Excellent package
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    *CRO/PHARMA EXPERIENCE REQUIRED*

    Skills Alliance are retained on a unique opportunity with an innovative vaccine organisation.

    The company specialises in vaccine development to combat epidemic outbreaks such as COVID and Ebola, they are a global partnership of government, civil society, philanthropic and Pharma organisations. They have a unique approach and will have a direct impact on global epidemics in the coming years. With this goal in mind, they are looking to build out the organisation and are looking for high calibre candidates who want to make a difference. They are very well funded and are an employer who is very focused on diversity.

    The Senior Project Manager will facilitate the successful delivery of several vaccine R&D projects associated with the organisation’s mission. Responsible to proactively manage all elements of each project – monitoring, scope, timelines, risk, budget and quality. They require previous cross-functional R&D project management experience, ideally managing projects from pre-clinical to commercialisation (phase I-III). They will consider experienced PMs from Pharma, Biotech or CRO and vaccines experience would be a strong preference.

    This is a full-time and permanent position to be home-based with regular travel to their offices in Central London when normality resumes. They will offer a very competitive salary – circa £60-80K depending on experience + full benefits package.

    Skills Alliance are the exclusive partner for this role, please get in contact with Mark Anderson for more details – +44 207 220 6209.

  • Clinical Operations

    £55000 - £65000 per annum, excellent package
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    A rare opportunity to join a growing Gene Therapies focussed Biotech. This is a permanent Senior Clinical Study Manager role based in Central London.

    This exciting and innovative Biotech company are at early stages with trials working in advanced therapies. They are expanding at present and will offer great long-term prospects. The company are looking for a very experienced Clinical Study Manager or Clinical Trial Manager, this would be working on complex and fast-paced studies from phase I-III. They require clinical trial management experience, ideally experience in early phase, complex TAs and interntional trial management expeirence. They have multiple programs ongoing and have a global presence.

    This is a full-time and permanent position. It is office-based in the London with flexibility to work from home (home-based during the pandemic). They offer an excellent salary and package around GBP 70-80K depending on experience + bonus + extensive benefits.

    Skills Alliance are the preferred supplier for this new Senior CPM / Senior CTM position. For more details please call Mark Anderson on 0207 220 6209 or click apply now.

  • Project Management

    £50000 - £60000 per annum, Excellent package
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    *PHARMA/BIOTECH EXPERIENCE REQUIRED*

    Skills Alliance are partnered to support a growing Biotech to hire for their Project Management team. The company are highly innovative and work in a new and exciting area, they have some exciting partnerships established and are growing rapidly. It is a fanastic time to join and they have a great team in place.

    The role will support the PMO to deliver clinical development projects and work closely with the R&D team. They are looking for someone at PM level who has strong Pharma/Biotech experience – ideally MS Project experience and a PRINCE2 or similar PM qualification would be a plus too. This is a new role due to a lot of expansion and exciting alliances they have running.

    The role is permanent, full-time and home-based initially, they would like someone to go into the Oxford office when normality resumes (with flexibility to WFH). They will offer circa £50-60K + bonus + benefits (may be some flex).

    Skills Alliance are pertnered to support the recruitment for this R&D Proejct Manager role. Please contact Mark Anderson for more info 0207 220 6209 or APPLY NOW.

  • Project Management

    £60000 - £75000 per annum, Excellent package
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    *CRO/PHARMA EXPERIENCE REQUIRED*

    Skills Alliance are retained on a unique opportunity with an innovative vaccine organisation.

    The company specialises in vaccine development to combat epidemic outbreaks such as COVID and Ebola, they are a global partnership of government, civil society, philanthropic and Pharma organisations. They have a unique approach and will have a direct impact on global epidemics in the coming years. With this goal in mind, they are looking to build out the organisation and are looking for high calibre candidates who want to make a difference. They are very well funded and are an employer who is very focused on diversity.

    The Vaccine Development Project Manager will facilitate the successful delivery of several vaccine R&D projects associated with the organisation’s mission. Responsible to proactively manage all elements of each project – monitoring, scope, timelines, risk, budget and quality. They require previous cross-functional R&D project management experience, ideally managing projects from pre-clinical to commercialisation (phase I-III). They will consider experienced PMs from Pharma, Biotech or CRO and vaccines experience would be a strong preference.

    This is a full-time and permanent position to be home-based with regular travel to their offices in Central London when normality resumes. They will offer a very competitive salary – circa £60-75K depending on experience + full benefits package.

    Skills Alliance are the exclusive partner for this role, please get in contact with Mark Anderson for more details – +44 207 220 6209.

  • Pre-Clinical

    £60000 - £65000 per annum, Bonus + benefits
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    A great opportunity to join a medium-sized CRO with a great culture and low turnover. They are recruiting for PM and Senior PM roles due to organic growth and new studies. *PHARMA EXPERIENCE REQUIRED*

    This company have a great track record and have been very successful during COVID where other CROs have struggled. They are a SME CRO who are dynamic and work in very interesting and complex therapy areas. Studies span phases I-IV and they work in Oncology and Gene Therapy amongst other areas.

    They are recruiting for multiple roles due to new studies coming in and they need an experienced cross-functional PM who has budget management experience. It could be working on a range of studies and would be working globally. There are also opportunities to progress quickly.

    This is a permanent and full-time role. They have an office in the South East but everyone is now home-based and this can be a remote role across the UK. They will offer a very good salary – GBP 60-65K + bonus + benefits.

    Skills Alliance are the preferred supplier for this new CPM / CTM position. For more details please call Mark Anderson on 0207 220 6209 or click apply now.

  • Project Management

    £60000 - £75000 per annum, Bonus + benefits
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    A great opportunity to join a medium-sized CRO with a great culture and low turnover. They are recruiting for PM and Senior PM roles due to organic growth and new studies. *PHARMA EXPERIENCE REQUIRED*

    This company have a great track record and have been very successful during COVID where other CROs have struggled. They are a SME CRO who are dynamic and work in very interesting and complex therapy areas. Studies span phases I-IV and they work in Oncology and Gene Therapy amongst other areas.

    They are recruiting for multiple roles due to new studies coming in and they need an experienced cross-functional PM who has strong budget management experience. It could be working on a range of studies and would be working globally. There are also opportunities to progress quickly.

    This is a permanent and full-time role. They have an office in the South East but everyone is now home-based and this can be a remote role across the UK. They will offer a very good salary – GBP 60-70K + bonus + benefits.

    Skills Alliance are the preferred supplier for this new CPM / CTM position. For more details please call Mark Anderson on 0207 220 6209 or click apply now.

  • Project Management

    £60000 - £75000 per annum, Excellent package
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    *CRO/PHARMA EXPERIENCE REQUIRED*

    Skills Alliance are retained on a unique opportunity with an innovative vaccine organisation.

    The company specialises in vaccine development to combat epidemic outbreaks such as COVID and Ebola, they are a global partnership of government, civil society, philanthropic and Pharma organisations. They have a unique approach and will have a direct impact on global epidemics in the coming years. With this goal in mind, they are looking to build out the organisation and are looking for high calibre candidates who want to make a difference. They are very well funded and are an employer who is very focused on diversity.

    The Senior Project Manager will facilitate the successful delivery of several vaccine R&D projects associated with the organisation’s mission. Responsible to proactively manage all elements of each project – monitoring, scope, timelines, risk, budget and quality. They require previous cross-functional R&D project management experience, ideally managing projects from pre-clinical to commercialisation (phase I-III). They will consider experienced PMs from Pharma, Biotech or CRO and vaccines experience would be a strong preference.

    This is a full-time and permanent position to be home-based with occassional travel to their offices in Central London when normality resumes. They will offer a very competitive salary – circa £60-£75K depending on experience + full benefits package.

    Skills Alliance are the exclusive partner for this role, please get in contact with Mark Anderson for more details – +44 207 220 6209.

  • Clinical Operations

    £50000 - £65000 per annum, bonus + benefits
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    I am partnered with an exciting Pharma client in the London area to help grow their Infectious Disease team.

    This growing Pharmaceutical company works across a range of areas of unmet medical need including Infectious Disease. They are a fantastic organisation who offer excellent development opportunities. Given their success in bringing products to market and rate of growth, this is a rare and exciting proposition. This is working in their Infectious Disease business unit.

    They are recruiting for a Clinical Study Manager to join the team and need an experienced and accomplished Project/Study Manager with international trial management experience. Pharma/Biotech experience is preferred but they will consider people from CRO. Infectious disease or vaccines experience would be a plus but not required.

    This is a full-time and permanent role, it would be home-based initially and they would want someone in the office several days per week post-COVID. The office is based in the London area. There is an excellent salary and package on offer – £50-65K depending on experience + bonus + benefits.

    Skills Alliance are the exclusive partner for this position, please get in touch with Mark Anderson to find out more on +44 207 220 6209 or APPLY NOW.

  • Clinical Operations

    £55000 - £65000 per annum, excellent package
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    A rare opportunity to join a growing Gene Therapies focussed Biotech. This is a permanent Senior Clinical Study Manager role based in Central London.

    This exciting and innovative Biotech company are at early stages with trials working in advanced therapies. They are expanding at present and will offer great long-term prospects. The company are looking for a very experienced Clinical Study Manager or Clinical Trial Manager, this would be working on complex and fast-paced studies from phase I-III. They require clinical trial management experience, ideally experience in early phase, complex TAs and interntional trial management expeirence. They have multiple programs ongoing and have a global presence.

    This is a full-time and permanent position. It is office-based in the London with flexibility to work from home (home-based during the pandemic). They offer an excellent salary and package around GBP 70-80K depending on experience + bonus + extensive benefits.

    Skills Alliance are the preferred supplier for this new Senior CPM / Senior CTM position. For more details please call Mark Anderson on 0207 220 6209 or click apply now.

  • Clinical Operations

    £65000 - £75000 per annum, Bonus + benefits
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    Great opportunity for an experienced Study Manager or Senior Study Manager to join a niche Bitoech working in advanced therapies. The role would be home-based initially with some travel to an office when normality resumes.

    The role is with a niche company who are very innovative and have exciting science. They company are growing quickly and have advanced therapies trials in early stages across several indications. This would be working at the cutting edge of research.

    The position is a wide ranging one given the size of the team. They need an autonomous Senior Clinical Study Manager who is keen to work in both science and operations. Early phase project management expeirence would be preferable and global experience.

    This is a permanent and full-time role. The role would be home-based initially with some travel to the office in the long-run. They offer an excellent salary + bonus.

    Skills Alliance are the preferred supplier for this role. Please contact Mark Anderson for more details – +44 207 220 6209 or click apply now.

  • Clinical Operations

    £60000 - £70000 per annum, Bonus + benefits
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    Great opportunity for a Study Manager or Senior Study Manager to join a niche Bitoech working in advanced therapies. The role would be home-based initially with some travel to an office when normality resumes!

    The role is with a niche company who are very innovative and have exciting science. They company are growing quickly and have advanced therapies trials in early stages across several indications. This would be working at the cutting edge of research.

    The position is a wide ranging one given the size of the team. They need an autonomous Clinical Study Manager who is keen to work in both science and operations. Early phase project management expeirence would be preferable.

    This is a permanent and full-time role. The role would be home-based initially with some travel to the office in the long-run. They offer an excellent salary + bonus.

    Skills Alliance are the preferred supplier for this role. Please contact Mark Anderson for more details – +44 207 220 6209 or click apply now.

  • Clinical Operations

    Very Competitive
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    Clinical Trial Assistant | Copenhagen
    An incredibly exciting Biotech are looking to onboard a pro-active Clinical Trial Assistant to be based in Copenhagen.
    This is a amazing opportunity to join a highly financially backed Biotech based out of Copenhagen who are currently going through a time of exciting growth and will continue to do so over the next few years. The CTA role would be in a small team where you would have the freedom to grow and develop as quickly as you wish, giving great opportunities for career progression.
    Responsibilities:

    • Provide administrative and operational support to all Clinical Operations.
    • Tracking and reporting on project timelines, budgets and deliverables.
    • Follow all studies from study start-up through study close-out.
    • Establish SOPs, ICH-GCP, and other applicable regulatory requirements across all tasks
    • Leading management of contracts with Sites and Vendors

    Requirements:

    • Previous experience within a CTA Role
    • In-depth knowledge of industry standards and best practices in clinical data management and ICH GCP.


    This Clinical Trial Assistant role is an flexible office based position based in Copenhagen

    Skills Alliance are the preferred supplier for this role. Please contact George Wykes for more details on +44 203 772 8236 or click APPLY NOW.

  • Clinical Development

    $29 - $36 per hour
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    We are actively partnered with a pioneering startup who are focused on making untreatable diseases, treatable. With an incredibly passionate team, they are looking to ensure that the patients with the worst outcomes are getting the best solutions possible.

    What you’ll do:

    • Utilize molecular biology skills (Cell Staining, DNA/RNA extraction, PCR)
    • Analyze data (Microsoft Office, GraphPad Prism, FlowJo) and present results to team members
    • Help in single cell suspension of tissue organs from mice
    • Characterize gene edited cells by flow cytometry, RT-QPCR, ELISA, Westernblot and other immunoassays

    What You’ll Bring:

    • Bachelor’s degree in related Life Sciences field
    • Team player, able to work with and adapt to the needs of different projects
    • Availability to work on occasional weekends
  • Commercial

    $29 - $36 per hour
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    We are representing a groundbreaking biotech startup who are dedicated to developing transformative medicines which can strike right at the heart of disease, while also focusing on keeping them broadly accessible to the patients who need them most!

    JOB DESCRIPTION

    Reporting to the Laboratory Facilities & Operations Manager, the Maintenance & Facilities Specialist III will primarily be involved with day-to-day facility operations and maintenance, including the establishment of continual improvement of utilities in laboratories. This person will work with the Laboratory Facilities & Operations team to maintain and improve laboratory functionality while upholding safety standards.
    Key responsibilities:

    • Maintaining service contracts for utilities and equipment, including: DI water systems, steam generator, autoclave, lab glassware washer, cold storage equipment, and lyophilizers
    • Overseeing environmental monitoring system for laboratory equipment and utilities
    • Coordinating installation of new utilities: a house CDA system, N2 and O2 generators for process gas lines, and a process chiller system
    • Routine maintenance of lab utilities, including: process gas manifolds (N2, CO2, O2) and water purification systems (Evoqua DI system, Elga & Millipore water polishers)
    • Liaising with vendors such as Praxair, Stericycle, Cintas, and Veolia for our laboratory services
    • Responding to laboratory facility emergencies, including occasional night or weekend availability should the need arise
  • Clinical Operations

    $48 - $62 per hour, Remote
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    We are actively partnered with a pioneering startup who are focused on making untreatable diseases, treatable. With an incredibly passionate team, they are looking to ensure that the patients with the worst outcomes are getting the best solutions possible.
    Looking to continue to grow and pursue their mission, they are in need of CRO Oversight and Reagent Development. This position will focus on the oversight of CRO based activities in support of gene and cell therapeutics. In this role, you will work on several gene and cell therapy programs, ensure that relevant assays are successfully transferred, qualified or validated at CROs and implemented for non-clinical and clinical study support.

    What You’ll Do:

    • Provide scientific and operational oversight of bioanalytical activities conducted at Contract Research Organizations (CROs), independently and in collaboration with a representative of the Dev Sci Bioanalytical group.
    • Provide scientific support to CRO efforts in design, development, and implementation of ligand binding, molecular, flow and other platform assays to determine analyte concentration, detect presence of immune response to drug product in a regulated (GLP, GCLP) environment
    • Work with Other members of the Dev Sci Bioanalytical group to ensure scientific rigor of analytical methods implemented and applied at CROs
    • Interface with CROs to ensure on time delivery of required milestones
    • Proactively communicate with the CRO to ensure transparence and adherence to the timelines, availability of required contracts, quotes, purchase orders, provide CRO with critical material, obtain and archive needed documentation, work with CRO to reconcile any scientific or operational concerns, manage standing review meetings, arrange vendor visits as appropriate

    What You’ll Bring:

    • Master’s degree or Bachelor’s degree with 7-10+ years of experience in industry setting, hands on GLP/GCLP experience, proven proficiency performing independent research.
    • Demonstrated experience working in regulated (GLP / GCLP) environment
    • Demonstrated experience managing CRO activities
  • Clinical Operations

    Very Competitive salary + Benefits
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    Clinical Trial Assistant | Copenhagen
    An incredibly exciting Biotech are looking to onboard a pro-active Clinical Trial Assistant to be based in Copenhagen.
    This is a amazing opportunity to join a highly financially backed Biotech based out of Copenhagen who are currently going through a time of exciting growth and will continue to do so over the next few years. The CTA role would be in a small team where you would have the freedom to grow and develop as quickly as you wish, giving great opportunities for career progression.
    Responsibilities:

    • Provide administrative and operational support to all Clinical Operations.
    • Tracking and reporting on project timelines, budgets and deliverables.
    • Follow all studies from study start-up through study close-out.
    • Establish SOPs, ICH-GCP, and other applicable regulatory requirements across all tasks
    • Leading management of contracts with Sites and Vendors

    Requirements:

    • Previous experience within a CTA Role
    • In-depth knowledge of industry standards and best practices in clinical data management and ICH GCP.


    This Clinical Trial Assistant role is an flexible office based position based in Copenhagen

    Skills Alliance are the preferred supplier for this role. Please contact George Wykes for more details on +44 203 772 8236 or click APPLY NOW.

  • Clinical Development

    £55000 - £75000 per annum, car allowance + bonus + benefits
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    I am partnered with a leading global Pharmaceutical company to hire multiple Clinical Scientist roles at Principal level – equivalent to Senior Manager / Associate Director. Home-based across the UK.

    This is a great opportunity to join a World-class Pharma company in their growing team which would be working globally. There are excellent development opportunities and the company is well established and has a great reputation.

    They need someone with excellent experience of writing clinical development plans and protocols. The role(s) are at the equivalent to Senior Manager / AD. The next step up would be Director level. They need significant clinical scientist experience but are flexible on background. A Masters or PhD would be preferred.

    The roles would be home-based in the UK or office-based in the South East. The office is based in the Surrey/London area. They will offer an excellent salary – £55-75K depending on level + car allowance + bonus + benefits.

    Skills Alliance are the exclusive partner for these roles. Please get in touch with Mark Anderson for more details +44 207 220 6209 or APPLY NOW.

  • Project Management

    £50000 - £60000 per annum, excellent package
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    A rare opportunity to join a fast growing Advanced Therapies focused Biotech. This is a permanent Clinical Trial Manager or Clinical Study Manager role based in the London area.

    This exciting and innovative Biotech company are at early stages with trials working in advanced therapies. They are expanding at present and will offer great long-term prospects. The company are looking for an experienced Junior Study Manager or Clinical Trial Manager, this would be working on interesting studies from phase I-III. They require a clinical trial management experience, ideally experience in early phase, complex TAs and experience of working with sites. They have multiple programs ongoing and have a global presence.

    This is a full-time and permanent position. It is office-based in the London area with flexibility to work from home (home-based during the pandemic). They offer an excellent salary and package around GBP 50-60K depending on experience + bonus + extensive benefits.

    Skills Alliance are the preferred supplier for this new CPM / CTM position. For more details please call Mark Anderson on 0207 220 6209 or click apply now.

  • Pre-Clinical

    £80000 - £90000 per annum, Excellent package
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    Senior Clin Ops role with an Oncology focussed Biopharma in the Oxfordshire area (home-based initially). Working at program level and leading their leading programs.

    This is a rare opportunity to join an exciting and fast-growing Oncology focused Biopharmaceutical company, they have a great pipeline spanning phase I-III and trials being run globally. They are growing and will offer excellent long-term opportunities. We have had excellent feedback from recent placements.

    They are recruiting for a Clinical Program Manager / AD role due to growth and new studies coming up, you would be leading their high profile programs in Oncology and they need a vastly experienced individual, ideally with Oncology trial management experience. They want someone who can work at a senior level and take on a leadership role in the team, line management if desired.

    The role is full-time, permanent and home-based initially, office-based in with flexibility when things return to normal in the Oxfordshire area. They will offer an excellent salary and package – around £80-90K basic salary + bonus + benefits + share options.

    Skills Alliance are the preferred partner for this role. Please get in touch with Mark Anderson for more details – 0207 220 6209.

  • Pre-Clinical

    £80000 - £90000 per annum, Excellent package
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    Associate Director, Clinical Operations role with an Oncology focussed Biopharma in the Oxfordshire area (home-based initially). Working at program level and leading their leading high profile programs.

    This is a rare opportunity to join an exciting and fast-growing Oncology focused Biopharmaceutical company, they have a great pipeline spanning phase I-III and trials being run globally. They are growing and will offer excellent long-term opportunities. We have had excellent feedback from recent placements.

    They are recruiting for a Clinical Program Manager / AD role due to growth and new studies coming up, you would be leading their high profile programs in Oncology and they need a vastly experienced individual, ideally with Oncology trial management experience. They want someone who can work at a senior level and take on a leadership role in the team, line management if desired.

    The role is full-time, permanent and home-based initially, office-based in with flexibility when things return to normal in the Oxfordshire area. They will offer an excellent salary and package – around £80-90K basic salary + bonus + benefits + share options.

    Skills Alliance are the preferred partner for this role. Please get in touch with Mark Anderson for more details – 0207 220 6209.

  • Pre-Clinical

    £45000 - £55000 per annum, Excellent package
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    Associate Clinical Study Manager role with an Oncology focussed Biopharma in the Oxfordshire area (home-based initially). Excellent progression opportunities.

    This is a rare opportunity to join an exciting and fast-growing Oncology focused Biopharmaceutical company, they have a great pipeline spanning phase I-III and trials being run globally. They are growing and will offer excellent long-term opportunities. We have had excellent feedback from recent placements.

    They are recruiting for a Junior Clinical Project Manager / Associate Clinical Study Manager role due to growth and new studies coming up, you would be supporting their high profile programs in Oncology and they need an experienced Junior PM or Lead CRA, ideally with some Oncology trial management experience. There will be opportunities to progress and gain international experience.

    The role is full-time, permanent and home-based initially, office-based in with flexibility when things return to normal in the Oxfordshire area. They will offer an excellent salary and package – around £45-55K basic salary + bonus + benefits.

    Skills Alliance are the preferred partner for this role. Please get in touch with Mark Anderson for more details – 0207 220 6209.

  • Clinical Operations

    £60000 - £90000 per annum, Bonus + benefits
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    Great opportunity for an experienced Clinical Project Manager or Study Manager to join Global Pharma company working in Oncology. The role would be home-based initially with some travel to the office when normality resumes.

    This is a great opportunity to join a World-class Pharma company with a great reputation and an excellent pipeline in Oncology, they are growing their Oncology division and it is an exciting time to join where you can expect fast progression opportunities. They are very patient centric and are innovative and science focussed.

    The role is a Clinical Project Manager / Clinical Trial Manager position managing studies across Europe and potentially globally. It is specifically in their Oncology division but they have other TAs too. Most of the studies are in phase II and III and they want people with commercial trial management, ideally in Oncology and some international experience.

    This is a permanent and full-time role. The role would be home-based initially with some travel to the London office further down the line. They offer an excellent salary in the region of £55-65K depending on experience + bonus + benefits.

    Skills Alliance are the exclusive partner for this role. Please contact Mark Anderson for more details – +44 207 220 6209 or click “APPLY NOW”.

  • Clinical Operations

    £50000 - £65000 per annum, bonus + benefits
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    I am partnered with an exciting Pharma client in the London area to help build out a new team in Oncology.

    This growing Pharmaceutical company works across a range of areas but is investing a lot in Oncology at present. They are a fantastic organisation who offer excellent development opportunities. Given their success in bringing products to market, rate of growth and the new team, this is a rare and exciting proposition. This is working in their Oncology business unit.

    They are recruiting for a Clinical Study Manager to join the team and need an experienced Project/Study Manager with some international trial management expeirence. Pharma/Biotech experience is preferred but they will consider people from CRO and significant Oncology experience is required (CRA or CTM level).

    This is a full-time and permanent role, it would be home-based initially and they would want someone in the office several days per week post-COVID. The office is based in the London area. There is an excellent salary and package on offer – £50-65K depending on experience + bonus + benefits.

    Skills Alliance are the exclusive partner for this position, please get in touch with Mark Anderson to find out more on +44 207 220 6209 or APPLY NOW.

  • Clinical Operations

    £55000 - £65000 per annum, excellent package
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    A rare opportunity to join a growing Gene Therapies focussed Biotech. This is a permanent Clinical Study Manager role based in Central London.

    This exciting and innovative Biotech company are at early stages with trials working in advanced therapies. They are expanding at present and will offer great long-term prospects. The company are looking for an experienced Clinical Study Manager or Clinical Trial Manager, this would be working on complex and fast-paced studies from phase I-III. They require a clinical trial management experience, ideally experience in early phase, complex TAs and interntional trial management expeirence. They have multiple programs ongoing and have a global presence.

    This is a full-time and permanent position. It is office-based in the London with flexibility to work from home (home-based during the pandemic). They offer an excellent salary and package around GBP 55-65K depending on experience + bonus + extensive benefits.

    Skills Alliance are the preferred supplier for this new CPM / CTM position. For more details please call Mark Anderson on 0207 220 6209 or click apply now.

  • Project Management

    £60000 - £75000 per annum, Excellent package
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    *CRO/PHARMA EXPERIENCE REQUIRED*

    Skills Alliance are retained on a unique opportunity with an innovative vaccine organisation.

    The company specialises in vaccine development to combat epidemic outbreaks such as COVID and Ebola, they are a global partnership of government, civil society, philanthropic and Pharma organisations. They have a unique approach and will have a direct impact on global epidemics in the coming years. With this goal in mind, they are looking to build out the organisation and are looking for high calibre candidates who want to make a difference. They are very well funded and are an employer who is very focused on diversity.

    The Vaccine Development Project Manager will facilitate the successful delivery of several vaccine R&D projects associated with the organisation’s mission. Responsible to proactively manage all elements of each project – monitoring, scope, timelines, risk, budget and quality. They require previous cross-functional R&D project management experience, ideally managing projects from pre-clinical to commercialisation (phase I-III). They will consider experienced PMs from Pharma, Biotech or CRO and vaccines experience would be a strong preference.

    This is a full-time and permanent position to be home-based with regular travel to their offices in Central London when normality resumes. They will offer a very competitive salary – circa £60-75K depending on experience + full benefits package.

    Skills Alliance are the exclusive partner for this role, please get in contact with Mark Anderson for more details – +44 207 220 6209.

  • Project Management

    £60000 - £75000 per annum, Excellent package
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    *CRO/PHARMA EXPERIENCE REQUIRED*

    Skills Alliance are retained on a unique opportunity with an innovative vaccine organisation.

    The company specialises in vaccine development to combat epidemic outbreaks such as COVID and Ebola, they are a global partnership of government, civil society, philanthropic and Pharma organisations. They have a unique approach and will have a direct impact on global epidemics in the coming years. With this goal in mind, they are looking to build out the organisation and are looking for high calibre candidates who want to make a difference. They are very well funded and are an employer who is very focused on diversity.

    The Senior Project Manager will facilitate the successful delivery of several vaccine R&D projects associated with the organisation’s mission. Responsible to proactively manage all elements of each project – monitoring, scope, timelines, risk, budget and quality. They require previous cross-functional R&D project management experience, ideally managing projects from pre-clinical to commercialisation (phase I-III). They will consider experienced PMs from Pharma, Biotech or CRO and vaccines experience would be a strong preference.

    This is a full-time and permanent position to be home-based with occassional travel to their offices in Central London when normality resumes. They will offer a very competitive salary – circa £60-£75K depending on experience + full benefits package.

    Skills Alliance are the exclusive partner for this role, please get in contact with Mark Anderson for more details – +44 207 220 6209.

  • Project Management

    £60000 - £77000 per annum, Bonus + benefits
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    A great opportunity to join a medium-sized CRO with a great culture and low turnover. They are recruiting for PM and Senior PM roles due to organic growth and new studies. *PHARMA EXPERIENCE REQUIRED*

    This company have a great track record and have been very successful during COVID where other CROs have struggled. They are a SME CRO who are dynamic and work in very interesting and complex therapy areas. Studies span phases I-IV and they work in Oncology and Gene Therapy amongst other areas.

    They are recruiting for multiple roles due to new studies coming in and they need an experienced cross-functional PM who has strong budget management experience. It could be working on a range of studies and would be working globally. There are also opportunities to progress quickly.

    This is a permanent and full-time role. They have an office in the South East but everyone is now home-based and this can be a remote role across the UK. They will offer a very good salary – GBP 60-77K + bonus + benefits.

    Skills Alliance are the preferred supplier for this new CPM / CTM position. For more details please call Mark Anderson on 0207 220 6209 or click apply now.

  • Clinical Operations

    £55000 - £65000 per annum, excellent package
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    A rare opportunity to join a growing Gene Therapies focussed Biotech. This is a permanent Senior Clinical Study Manager role based in Central London.

    This exciting and innovative Biotech company are at early stages with trials working in advanced therapies. They are expanding at present and will offer great long-term prospects. The company are looking for a very experienced Senior Clinical Study Manager or Senior Clinical Trial Manager, this would be working on complex and fast-paced studies from phase I-III. They require substantial clinical trial management experience, ideally experience in early phase, complex TAs and international trial management experience. They have multiple programs ongoing and have a global presence.

    This is a full-time and permanent position. It is office-based in the London with flexibility to work from home (home-based during the pandemic). They offer an excellent salary and package around GBP 70-80K depending on experience + bonus + extensive benefits.

    Skills Alliance are the preferred supplier for this new Senior CPM / Senior CTM position. For more details please call Mark Anderson on 0207 220 6209 or click apply now.

  • Clinical Operations

    £50000 - £65000 per annum, bonus + benefits
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    I am partnered with an exciting Pharma client in the London area to help grow their Infectious Disease team.

    This growing Pharmaceutical company works across a range of areas of unmet medical need including Infectious Disease. They are a fantastic organisation who offer excellent development opportunities. Given their success in bringing products to market and rate of growth, this is a rare and exciting proposition. This is working in their Infectious Disease business unit.

    They are recruiting for a Clinical Study Manager to join the team and need an experienced and accomplished Project/Study Manager with international trial management experience. Pharma/Biotech experience is preferred but they will consider people from CRO. Infectious disease or vaccines experience would be a plus but not required.

    This is a full-time and permanent role, it would be home-based initially and they would want someone in the office several days per week post-COVID. The office is based in the London area. There is an excellent salary and package on offer – £50-65K depending on experience + bonus + benefits.

    Skills Alliance are the exclusive partner for this position, please get in touch with Mark Anderson to find out more on +44 207 220 6209 or APPLY NOW.