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    My client is a global biopharmaceutical company leading in rare diseases, with a diverse and further expanding product portfolio focused on transforming biopharmaceutical discoveries into novel medicines.

    If you are looking to take part in a value driven organisation dedicated to improving patients’ lives, and be a game changer in determining access to life-changing medicines, for those with limited or no options,

    Responsibilities:

    As part of the portfolio expansion into a new rare diseases therapeutic area, your goal will be to secure positive recommendations for the new novel medicines through full management of the Health Technology Assessment (HTA) across the UK. This includes the national institute for health care excellence (NICE), National centre for Pharmacoeconomics and the Scottish Medicines Consortium.

    Responsible for the delivery of HTA submissions to the relevant authorities, the management of the projects initially in UK and Ireland with scope to develop to full EU and Global coverage considering the exponential growth of the companies leading drugs.

    Act as the first and main point of contact on HTA? reimbursement projects and facilitate internal and external stakeholders to a positive decision outcome.

    Identification and tracking of strategic decisions required for HTA

    Lead coordination of dossiers, prepare, submit and follow up pricing and reimbursement

    Liaise across a wide network of internal and external stakeholders both local and global to ensure market access objectives are met.

    Requirements:

    Prior experience of developing submissions with understanding and familiarity with NICE/SMC/NCPE appraisal processes

    Understanding of a complex disease area and ability to quickly grasp complex HTA decisions from this

    Ability to rapidly assimilate and translate complex problems into practical and deliverable solutions

    Stakeholder management skills (Internal and external) with the ability to liaise at all levels in an organisation with credibility and impact

    Strong project management with the ability to co-ordinate cross functional teams and evidenced through project management qualification

    You are intellectually curious, self- motivated and tenacious

    Degree in health/ sciences or economics related discipline and formal project management training/ accreditation

    What to do now?
    The aforementioned role is within a highly niche therapeutic area making this position highly desirable and competitive on the market. I advise you get in contact ASAP by applying, or you can reach out directly through my direct line below and Linkedin message.
    M: +44 0207 220 6224

    I am networking on behalf of global pharmaceutical companies as well as niche biotech and medical devices, specialising in commercial executive search. Get in contact for a confidential discussion on your career goals and how my network can benefit.

  • €200000 - €250000 per annum
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    Unser Klient führt mehrere Krankenhäuser in der Schweiz. Das ganze medizinische Spektrum wird an allen Standorten verteilt angeboten.

    Zur verstärkung des Teams suchen wir deshalb noch ein/e Leitender Arzt / Leitende Ärztin für die Pneumolgie.

    Was Sie erwartet:

    • Co-Leitung der Abteilung für Pneumolgie mit Aussicht auf Gesamtleitung
    • Sie decken das ganze Spektrum der klinischen Pneumologie ab
    • Weiterbildung des Personals

    Was Sie mitbringen:

    • Facharzttitel für Pneumologie
    • Fähigkeitsausweis Schlafmedizin
    • Erfahrung in einer Kaderposition ist erzwingend
    • Ausgezeichnete Kenntnisse im Bereich der gesamten Innere Medizin

    Ihre Vorteile

    • attraktive Karrieremöglichkeiten
    • motivierendes Arbeitsklima
    • hohe Qualitätsstandards

    Diskretion steht bei uns an erster Stelle. In einem vertraulichen Gespräch geben wir Ihnen gerne mehr Auskunft über die Position.

    Jessica Demirtas
    Recruitment & Consultant DACH
    +41 43 508 73 11
    jessica.demirtas(at)skillsalliance.com

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    This is an excellent opportunity to join one of the most exciting global gene therapy companies in the Greater Boston area with a robust late stage pipeline offering rapid career progression. As the Senior Director of Clinical Operations, you will initially take on an operationally focused role managing and implementing the foundation of a ground-breaking product launch.

    Reporting directly into the VP of Clinical Operations,you will have a rare opportunity to work side by side and gain exposure to the pre-clinical stage of the clinical trial.In this role, you will be responsible for overseeing and leading the delivery and execution of the operations for the brand-new product launch. This will include collaborating externally cross-functionally with internal and global teams.

    You must have a minimum of a bachelor’s degree and a minimum of 12 years of clinical operations experience in a pharmaceutical or biotech setting. A gene therapy background a strong personality would be looked at favorably.

    The company is one of the most unique in the industry with a proven track record of success both domestic and abroad in the gene therapy space. This is the right time to be joining this truly innovative team!

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    This is an excellent opportunity to join one of the most exciting global Biotech’s in the Greater Boston area with a recent product launch in the rare disease therapeutic area. As the Director of Medical Communication, you will lead the publication planning and strategy for this ground-breaking product launch. The successful applicant will have the chance to have a leadership role and have an influential position in the organization.

    Reporting to the Senior Director Global Medical Communications, the applicant will have the opportunity to manage the Global Medical Communication team. You will be responsible for creating executing global medical communication strategy and creating high quality and impact global resources that communicate relevant disease-state data for this company’s therapeutics. You will work cross-functional and cross-geographic with partners including the Global Medical Affairs Leads and Clinical Development to inform and execute medical strategies. The successful candidate will be responsible for the development of medical communication resources aligned to global strategy for the company’s therapeutic.

    You must have a minimum of an advanced degree in biomedical sciences (PhD, MD or PharmD), and a minimum of two years of relevant experience in Medical Affairs and/or Medical Communication in a pharmaceutical or biotech setting. A background in the rare disease therapeutic area would be looked at favorably. The company is one of the most unique in the industry with a proven track record of success in the rare disease space. This is the right time to be joining this truly innovative team!

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    A leading pharmaceutical company are recruiting for a Senior Marketing Manager (Cardiology) in London. You would be responsible in developing and implementing a marketing strategy for UK and European Markets. You will work with and report into the business unit head. You will create solid customer relationships assembled on your perception of their requirements and your capacity to demonstrate your integrity by filling those requirements.
    You will exhibit a high degree of knowledge within your specialist therapeutic area and utilize a variety of promotional strategies to successfully execute them. Contributing to the marketing/brand teams and wider account teams you work within, whilst building and securing business strategies and conveying them successfully.

    The role is office based. It’s a permanent role offering an excellent package with a competitive salary.

    Skills Alliance are the preferred supplier for this role. Please contact Warda Issa for more details on +44 203 823 4158.

  • UK

    £60000 - £70000 per annum
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    I am currently recruiting for a Senior Medical Writer role for a global CRO focussing on Oncology. This role will involve dealing with regulatory and clinical trial submissions along with clinical and non-clinical publications and will offer flexible home-working and a very competitive salary and package.

    Skills Alliance are the preferred supplier for this role please reach out to Silvia Gullone on 02072206219

  • £20000 - £250000 per annum
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    A GMP focused pharmaceutical manufacturing company is looking for a Quality Officer to join their team. This role will allow you to work within a strong team to maintain and promote a good quality culture within the company.

    This company has recently won new projects that will expand the scope of its current manufacturing portfolio. They have been working with existing pharmaceutical companies over a number of years and have expected growth forecast for the next year.

    This role will be open to graduates who have a relevant degree with a scientific background who have encountered aspects of cGMP and have relevant experience working with Quality Management Systems. Individuals with relevant Quality experience within life sciences or medical devices are also desirable.

    The salary is £20,000 – £25,000K dependent on experience. If you are interested in hearing more about this role please contact Lauren Lonsdale on 02072206229.

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    Skills Alliance are partnered with an International Medical device/engineering company based in the German part of Switzerland. For this purpose, our client will be looking for a Clinical Project Leader to join their team and this is a permanent role.

    Job Qualifications:-

    • Project management responsibility for a clinical project targeting an FDA premarket approval (PMA) of a strategic and innovative medical device product
    • Conduction and oversight of a multi-center (Europe and US) randomized controlled trial within planned timeline and budget
    • Management of a CRO
    • Definition and co-authoring all essential clinical study documentation as required by the FDA and local legal requirements (ethical committees and IRBs)
    • Keeping a close contact with clinical investigators and sites in Europe and US, regularly visiting them (substantial amount of business travel time)
    • Willingness to travel up to 50% of your working time

    Job REQUIREMENTS:-

    • NPD or Product launch experience is required
    • Class III implantable experience is required i.e. examples of Class III devices include implantable pacemaker, pulse generators, HIV diagnostic tests, automated external defibrillators, and endosseous implants.
    • Knowledge of MDR
    • Experience in international medical device regulations; relevant guidelines-knowledge of FDA PMA
    • Experience in communicating with regulatory authorities, specifically FDA is a must
    • Masters or Bachelors degree in science or medicine
    • Advanced degree MD or PhD is preferred
    • English is required, any other languages would be an asset

    For more information please contact Heena Verma @ +41 (0)447982410

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    Skills Alliance are partnered with an International Medical device/engineering company based in the German part of Switzerland. For this purpose, our client will be looking for a Clinical Project Leader to join their team and this is a permanent role.

    Job Qualifications:-

    • Project management responsibility for a clinical project targeting an FDA premarket approval (PMA) of a strategic and innovative medical device product
    • Conduction and oversight of a multi-center (Europe and US) randomized controlled trial within planned timeline and budget
    • Management of a CRO
    • Definition and co-authoring all essential clinical study documentation as required by the FDA and local legal requirements (ethical committees and IRBs)
    • Keeping a close contact with clinical investigators and sites in Europe and US, regularly visiting them (substantial amount of business travel time)
    • Willingness to travel up to 50% of your working time

    Job REQUIREMENTS:-

    • NPD or Product launch experience is required
    • Class III implantable experience is required i.e. examples of Class III devices include implantable pacemaker, pulse generators, HIV diagnostic tests, automated external defibrillators, and endosseous implants.
    • Knowledge of MDR
    • Experience in international medical device regulations; relevant guidelines-knowledge of FDA PMA
    • Experience in communicating with regulatory authorities, specifically FDA is a must
    • Masters or Bachelors degree in science or medicine
    • Advanced degree MD or PhD is preferred
    • English is required, any other languages would be an asset

    For more information please contact Heena Verma @ +41 (0)447982410

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    Share

    Skills Alliance are partnered with an International Medical device/engineering company based in the German part of Switzerland. For this purpose, our client will be looking for a Clinical Project Leader to join their team and this is a permanent role.

    Job Qualifications:-

    • Project management responsibility for a clinical project targeting an FDA premarket approval (PMA) of a strategic and innovative medical device product
    • Conduction and oversight of a multi-center (Europe and US) randomized controlled trial within planned timeline and budget
    • Management of a CRO
    • Definition and co-authoring all essential clinical study documentation as required by the FDA and local legal requirements (ethical committees and IRBs)
    • Keeping a close contact with clinical investigators and sites in Europe and US, regularly visiting them (substantial amount of business travel time)
    • Willingness to travel up to 50% of your working time

    Job REQUIREMENTS:-

    • NPD or Product launch experience is required
    • Class III implantable experience is required i.e. examples of Class III devices include implantable pacemaker, pulse generators, HIV diagnostic tests, automated external defibrillators, and endosseous implants.
    • Knowledge of MDR
    • Experience in international medical device regulations; relevant guidelines-knowledge of FDA PMA
    • Experience in communicating with regulatory authorities, specifically FDA is a must
    • Masters or Bachelors degree in science or medicine
    • Advanced degree MD or PhD is preferred
    • English is required, any other languages would be an asset

    For more information please contact Heena Verma @ +41 (0)447982410

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    Job
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    Skills Alliance are partnered with an International Medical device/engineering company based in the German part of Switzerland. For this purpose, our client will be looking for a Clinical Project Leader to join their team and this is a permanent role.


    Job Qualifications:-

    • Project management responsibility for a clinical project targeting an FDA premarket approval (PMA) of a strategic and innovative medical device product
    • Conduction and oversight of a multi-center (Europe and US) randomized controlled trial within planned timeline and budget
    • Management of a CRO
    • Definition and co-authoring all essential clinical study documentation as required by the FDA and local legal requirements (ethical committees and IRBs)
    • Keeping a close contact with clinical investigators and sites in Europe and US, regularly visiting them (substantial amount of business travel time)
    • Willingness to travel up to 50% of your working time


    Job REQUIREMENTS:-

    • NPD or Product launch experience is required
    • Class III implantable experience is required i.e. examples of Class III devices include implantable pacemaker, pulse generators, HIV diagnostic tests, automated external defibrillators, and endosseous implants.
    • Knowledge of MDR
    • Experience in international medical device regulations; relevant guidelines-knowledge of FDA PMA
    • Experience in communicating with regulatory authorities, specifically FDA is a must
    • Masters or Bachelors degree in science or medicine
    • Advanced degree MD or PhD is preferred
    • English is required, any other languages would be an asset


    For more information please contact Heena Verma @ +41 (0)447982410 or email at

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    Antibody Engineer

    Our client, a leading pharmaceutical company are looking for an Antibody Engineer to join their dynamic and vastly growing team ahead of multiple launches. Thanks to extensive investment to their drug development department they have multiple products across their pipeline. They specialise their work within Antibody/Protein Engineering and have already received very promising results for their ground-breaking research. The individual will play a leading role in the discovery and development of treatments and cures for HIV. The position is based in North Carolina, but offers a generous relocation package for those currently living further away.

    The Role

    In order to be successful in this position you must have excellent leadership and communication skills and be capable of working on multiple assignments simultaneously. The main area of focus will be on advancing treatment, prevention and cure for HIV, so your work will have a direct impact on the lives of many patients. The company are leaps and bounds of the competition in this sector and are on the verge of changing the way the world thinks about HIV. The role will be primarily lab based however it offers some flexibility around working from home, and comes with a very competitive salary and bonus package.

    Responsibilities:

    – Discovery of the properties of different antibodies and assessment of potential application to HIV treatment.

    – Using molecular biology techniques to produce antibodies for this project.

    – Working independently and as part of the project team while ensuring you can effectively understand and communicate the complex scientific data you discover.

    Requirements:

    – PhD or MS in Molecular/Cellular Biology or Protein Engineering

    – With PhD must have 2-5 years of relevant pharmaceutical or academic experience, or 5-10 years with MS.

    Apply:

    Apply here if you are interested in this opportunity or if you would like a confidential discussion about your career opportunities please contact: matthew.t.a4lgdx1gsjdi@skillsalliance.aptrack.co or +44 (0) 20 7220 6200

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    Skills Alliance are partnered with an International CRO that is currently expanding their CRA group. For this purpose, our client will be looking for multiple Freelance Clinical Research Associates to join their team in Austria.

    If you are a Clinical Research Associate with at least 2-4 years of monitoring experience and are looking for a new opportunity, then feel free to get in touch.

    REQUIREMENTS

    A Bachelor’s degree in natural / life science, pre-medicine, nursing, bio-engineering, or a related field

    Minimum 2 years clinical research experience

    Strong written and verbal communication skills and the ability to interpret basic clinical data

    Basic IT Skills (i.e., word processing software and relevant clinical applications)

    Ability to work independently in a global team environment and to exchange straightforward information

    Proficient level of German and English

    Relevant certification by an industry-recognized professional society

    For more information please contact Heena Verma at +41 (0) 44 798 2410

  • Competitive
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    Skills Alliance are partnered with an International CRO that is currently expanding their CRA group. For this purpose, our client will be looking for multiple Freelance Clinical Research Associates to join their team in Switzerland.

    If you are a Clinical Research Associate with at least 2-4 years of monitoring experience and are looking for a new opportunity, then feel free to get in touch.

    REQUIREMENTS

    A Bachelor’s degree in natural / life science, pre-medicine, nursing, bio-engineering, or a related field

    Minimum 2 years clinical research experience

    Strong written and verbal communication skills and the ability to interpret basic clinical data

    Basic IT Skills (i.e., word processing software and relevant clinical applications)

    Ability to work independently in a global team environment and to exchange straightforward information

    Proficient level of German and English

    Relevant certification by an industry-recognized professional society

    For more information please contact Heena Verma at +41 (0) 44 798 2410

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    Skills Alliance are partnered with an International CRO that is currently expanding their CRA group. For this purpose, our client will be looking for multiple Freelance Clinical Research Associates to join their team in Germany.

    If you are a Clinical Research Associate with at least 2-4 years of monitoring experience and are looking for a new opportunity, then feel free to get in touch.

    REQUIREMENTS

    A Bachelor’s degree in natural / life science, pre-medicine, nursing, bio-engineering, or a related field

    Minimum 2 years clinical research experience

    Strong written and verbal communication skills and the ability to interpret basic clinical data

    Basic IT Skills (i.e., word processing software and relevant clinical applications)

    Ability to work independently in a global team environment and to exchange straightforward information

    Proficient level of German and English.

    Relevant certification by an industry-recognized professional society

    For more information please contact Heena Verma at +41 (0) 44 798 2410

  • €110000 - €120000 per annum, Bonus
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    Skills Alliance is partnered with a medical device company that specialises in oncology. On our client’s behalf, we are currently recruiting for a Senior Quality Assurance Engineer to join our client’s team close to Luzern, Switzerland. In this role you will ensure the compliance of our client’s products and product documentation throughout the product life cycle.

    Responsibilities:
    – Provide guidance to project teams
    – Define and ensure quality requirements in development projects
    – Risk analysis and FMEAs
    – CAPA management
    – Customer / Internal / Regulatory audits
    – Development of the management system (ISO 13485)
    – Implementation of MDR

    Requirements:
    – University degree in Engineering or Science
    – 5+ years of experience in quality or compliance in the medical device industry
    – Experience in the FMEA method
    – Knowledge in implementing and interpreting regulatory requirements (MDD/MDR, ISO 13485, ISO 14971, FDA 21 CFR 820)
    – Proficiency in English & German

    Please note that only citizens of EU/EFTA member states can be considered.
    If you have any questions regarding this position, please contact Khephren Mongongu +41 43 508 29 16 for more information. We are looking forward to your application.

  • €100000 - €120000 per annum, Bonus
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    Skills Alliance is currently partnered with a medium sized medical device company with an important presence across Germany and the EU. Our client’s products are crucial to protect patients at hospitals across the world. With a strong portfolio of marketed products and an impressive pipeline, the Senior Manager Quality vacancy is a great opportunity to join a company that has sustained high levels of growth year after year.

    In this position, you will be developing and implementing a strong quality strategy for our client’s operations across your designated region. You will be interacting with key business stakeholders and make sure regional affiliates comply to the company’s quality management system. You will also be a leading company figure for compliance to the EU MDR.

    Requirements
    – Bachelor’s in a life science related field or engineering degree
    – 10+ years of experience in the medical device industry
    – 5 years of managerial experience in business/corporate or supplier quality
    – Quality certification (ISO internal/external auditor, Six Sigma or similar)
    – Fluency in English and German

    For more information on this role, please contact Khephren Mongongu +41 (0) 43 508 29 16. We are looking forward to your application.

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    Clinical Research Associate

    Location: Germany
    Job Type: Contract

    Skills Alliance is partnered with an International CRO that is seeking a Clinical Research Associate to join their team in Germany. For this purpose, we are currently supporting our client in their search.

    If you are a Clinical Research Associate with at least 4 years of monitoring experience and are looking for a new opportunity, then feel free to get in touch.

    Main responsibilities:

    • Managing all aspects of study development such as organization, scope, design, execution, monitoring, and study documentation
    • Acting as the main link between the sponsor company and the parties involved in the study
    • Ensuring clinical examination according to GCP guidelines

    Education and Experience Requirements:

    • A Bachelor’s/Master’s degree in Life Sciences or equivalent training/experience
    • 3-4 years of experience in clinical research
    • Experience in clinical studies within Oncology, Immunology, Cardiology etc
    • Fluent in English and German
    • Ability and willingness to travel

    Contact person: Egi Bendo +41 43 508 21 04

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    Skills Alliance are partnered with an International CRO that is currently expanding their CRA group. For this purpose, our client will be looking for multiple Freelance Clinical Research Associates to join their team in Italy.

    If you are a Clinical Research Associate with at least 2-4 years of monitoring experience and are looking for a new opportunity, then feel free to get in touch.

    REQUIREMENTS

    • A Bachelor’s degree in natural / life science, pre-medicine, nursing, bio-engineering, or a related field
    • Minimum 2 years clinical research experience
    • Strong written and verbal communication skills and the ability to interpret basic clinical data
    • Basic IT Skills (i.e., word processing software and relevant clinical applications)
    • Ability to work independently in a global team environment and to exchange straightforward information
    • Proficient level of English
    • Relevant certification by an industry-recognized professional society

    For more information please contact Vasil Mihaylov at +41 (0) 435 086 961

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    This is an excellent opportunity to join one of the most exciting global gene therapy companies in the Greater Boston area with a robust late stage pipeline offering rapid career progression. Our client is one of the most unique in the industry with a proven track record of success both domestic and abroad in the gene therapy space.

    The Role

    As the Associate Director of CMC Regulatory Affairs, you will take on a role planning, preparing, and reviewing CMC related submission documentation.

    Reporting directly into the Global Head of CMC, the applicant will be overseeing and leading the delivery and execution of the CMC submissions. You will have the opportunity to lead contributions on INDs for their assets that are being submitted in the next year. Also, you will be responsible for submitting NDAs for their assets in that are in later phases.

    Requirements:

    – You must have a minimum of a bachelor’s degree

    – A minimum of 10 years of regulatory affairs experience in a pharmaceutical or biotech setting

    – Oncology background and a strong personality would be looked at favorably

    Apply here If you are interested in this opportunity and would like more information on this role.