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  • Clinical Operations

    £80000 - £95000 per annum, Excellent package
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    Senior Clin Ops role with an Oncology focussed Biopharma in London. Working at program level and leading their leading programs and line managing a small team.

    This is a rare opportunity to join a reputable Biopharmaceutical company with a great reputation, 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, with Oncology trial management and line management experience. They want someone who can work at a senior level and take on a leadership role in the team. It could be haematology or solid tumours.

    The role is full-time, permanent and home-based initially, office-based (2 days) with flexibility when things return to normal in London. They will offer an excellent salary and package – around £80-905K basic salary + bonus + benefits + stock.

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

  • Clinical Development

    £60000 - £80000 per annum, Bonus + benefits
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    *PHARMA EXPERIENCE REQUIRED*

    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 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 60-80K + 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

    £75000 - £110000 per annum, excellent package
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    A very exciting opportunity to join a growing Biopharma. Permanent Late Phase Clinical Program Manager / Associate Director role based in London offering an excellent salary and package.

    This exciting and innovative Biopharma have many products on the market and a very strong pipeline. They will be expanding and will offer great long-term prospects. The company are looking for an experienced Program Manager or Associate Director, this would be working on a variety of late phase phase studies. They require a substiantial clinical trial / program management background and strong and recent non-interventional / observational trials experience. Line management is also essential as it will be managing a smal but growing team.

    This is a full-time and permanent position. It is based in West London with lots of flexibility to work from home. They offer an excellent salary and package around GBP 75-110K depending on experience + bonus + extensive benefits + stock.

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

  • Clinical Development

    £80000 - £110000 per annum, Excellent package
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    SENIOR MANAGER / ASSOCIATE DIRECTOR, CLINICAL DEVELOPMENT – SMALL AND FAST GROWING BIOTECH – OXFORD

    This is a great opportunity to join a fast-growing Biotech who do very exciting work in the advanced therapies space. They are doing work across multiple therapy areas at present. This is a superb time to join as they are advancing into phase III studies with their leading program but also other trials in early phase. The organisation also has some exciting collaborations ongoing.

    The role is a senior clinical development scientist position, they are flexible on level and need an experienced clinical development professional who has good experience of writing and developing clin dev plans and protocols or someone with a Medic/Pharmacist background with medical monitoring experience. It reports into the Medical Director for the TA and is the only role in the team right now so lots of scope for development and progression in the future. They are flexible on TA experience and would prefer experience across phases I-III.

    This is a full-time and permanent role. The company is based in Oxford and they would like someone to be there 3 days per week ideally. They will offer a very good salary and it would depend on the level – around £80-110K depending on experience + bonus + benefits + shares.

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

  • Pre-Clinical

    £60000 - £80000 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 60-80K + 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 Development

    £70000 - £90000 per annum, Excellent package
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    SENIOR MANAGER / ASSOCIATE DIRECTOR, CLINICAL DEVELOPMENT – SMALL AND FAST GROWING BIOTECH – OXFORD

    This is a great opportunity to join a fast-growing Biotech who do very exciting work in the advanced therapies space. They are doing work across multiple therapy areas at present. This is a superb time to join as they are advancing into phase III studies with their leading program but also other trials in early phase. The organisation also has some exciting collaborations ongoing.

    The role is a senior clinical development scientist position, they are flexible on level and need an experienced clinical development professional who has good experience of writing and developing clin dev plans and protocols or someone with a Medic/Pharmacist background with medical monitoring experience. It reports into the Medical Director for the TA and is the only role in the team right now so lots of scope for development and progression in the future. They are flexible on TA experience and would prefer experience across phases I-III.

    This is a full-time and permanent role. The company is based in Oxford and they would like someone to be there 3 days per week ideally. They will offer a very good salary and it would depend on the level – around £70-90K depending on experience + bonus + benefits + shares.

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

  • Clinical Operations

    £85000 - £100000 per annum, excellent package
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    A very exciting opportunity to join a growing Biopharma. Permanent Late Phase / Observational Associate Director, Clinical Operations role based in London (lots of home working) offering an excellent salary and package. It is a very senior role within the department.

    This exciting and innovative Biopharma have many products on the market and a very strong pipeline. They will be expanding and will offer great long-term prospects. The company are looking for an experienced Program Manager or Associate Director, this would be working on a variety of late phase phase studies. They require a substiantial clinical trial / program management background and strong and recent non-interventional / observational trials experience. Line management is also essential as it will be managing a small but growing team.

    This is a full-time and permanent position. It is based in West London with lots of flexibility to work from home. They offer an excellent salary and package around GBP 85-100K depending on experience + car allowance + bonus + extensive benefits + stock.

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

  • Clinical Operations

    £65000 - £75000 per annum, Excellent package
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    Senior Global Clinical Study Manager position – purely working in Oncology, could be solid tumours or haematology. Study responsibility and line management of a small team.

    This is a great opportunity to join a reputable Biopharmaceutical company with a great reputation, they have a great pipeline spanning phase I-III and trials being run globally. They are growing and will offer excellent long-term opportunities. They are investing a huge amount in Oncology at present and we have had excellent feedback from recent placements.

    They are recruiting for a Senior Clinical Study Manager / Senior Global Trial Manager 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, with Oncology trial management and line management experience. They want someone who can work at a senior level and take on a leadership role in the team. It could be haematology or solid tumours.

    The role is full-time, permanent and home-based initially, office-based (2 days) with flexibility when things return to normal in London. They will offer an excellent salary and package – around £65-75K basic salary + excellent bonus + benefits + stock.

    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 - £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 - £78000 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

    €60000 - €75000 per annum, + benefits + bonus
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    Job
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    You are currently registered and logged onto our site and this form is therefore using the personal details and CV you have saved with your profile. You can amend them here but they won't overwrite your saved account details. The new uploaded CV and/or cover letter will be saved onto your account if it is not exceeding the maximum of 5 documents.

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    Europe Clinical Project Manager – Home based in Europe
    A US based, Global CRO, specialising in the generation, analysis and communication of real-world evidence throughout the product lifecycle.
    This is a great opportunity to join a rapidly growing SME CRO, with major developments coming within the EU in recent years, following its re-establishment as a standalone provider of pharmaceutical services. With this expansion, there are great opportunities for professional development and progression. They work within evidence-based research with a primary focus on rare disease, novel indications, and speciality therapies.
    Responsibilities:

    • Operational oversight of projects, acting as leading role in planning, coordinating, and completing project work
    • Work closely with the internal and external stakeholders, such as internal project team members, vendors, and suppliers to ensure success in assigned projects.
    • Management of deliverables and timelines
    • Bid defences, pitching to external pharma and biotech
    • Budgeting and change order responsibilities

    Requirements:

    • Full-service project management experience.
    • Several years Project Management experience within a CRO.
    • International experience managing global projects.

    This Clinical Project Manager role is a home-based role in Spain. It is a permanent role offering around €60K-€75K+ bonus + benefits.

    Skills Alliance are the exclusive partner for this role. Please contact Filip Szurkiewicz for more details on +44 203 910 1229 or click APPLY NOW.

  • Clinical Operations

    €60000 - €75000 per annum, + benefits + bonus
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    Job
    Application

    You are currently registered and logged onto our site and this form is therefore using the personal details and CV you have saved with your profile. You can amend them here but they won't overwrite your saved account details. The new uploaded CV and/or cover letter will be saved onto your account if it is not exceeding the maximum of 5 documents.

    Before applying for this position you need to submit your online CV. Click the button below to continue.


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    Europe Senior Clinical Project Manager – Home based in Europe
    A US based, Global CRO, specialising in the generation, analysis and communication of real-world evidence throughout the product lifecycle.
    This is a great opportunity to join a rapidly growing SME CRO, with major developments coming within the EU in recent years, following its re-establishment as a standalone provider of pharmaceutical services. With this expansion, there are great opportunities for professional development and progression. They work within evidence-based research with a primary focus on rare disease, novel indications, and speciality therapies.
    Responsibilities:

    • Operational oversight of projects, acting as leading role in planning, coordinating, and completing project work
    • Work closely with the internal and external stakeholders, such as internal project team members, vendors, and suppliers to ensure success in assigned projects.
    • Management of deliverables and timelines
    • Bid defences, pitching to external pharma and biotech
    • Budgeting and change order responsibilities

    Requirements:

    • Full-service project management experience.
    • Several years Project Management experience within a CRO.
    • International experience managing global projects.

    This Senior Clinical Project Manager role is a home-based role in Spain. It is a permanent role offering around €60K-€75K+ bonus + benefits.

    Skills Alliance are the exclusive partner for this role. Please contact Filip Szurkiewicz for more details on +44 203 910 1229 or click APPLY NOW.

  • Clinical Operations

    €75000 - €90000 per annum, + benefits + bonus
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    Job
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    You are currently registered and logged onto our site and this form is therefore using the personal details and CV you have saved with your profile. You can amend them here but they won't overwrite your saved account details. The new uploaded CV and/or cover letter will be saved onto your account if it is not exceeding the maximum of 5 documents.

    Before applying for this position you need to submit your online CV. Click the button below to continue.


    Share

    Europe Clinical Project Manager – Home based in Europe
    A US based, Global CRO, specialising in the generation, analysis and communication of real-world evidence throughout the product lifecycle.
    This is a great opportunity to join a rapidly growing SME CRO, with major developments coming within the EU in recent years, following its re-establishment as a standalone provider of pharmaceutical services. With this expansion, there are great opportunities for professional development and progression. They work within evidence-based research with a primary focus on rare disease, novel indications, and speciality therapies.
    Responsibilities:

    • Operational oversight of projects, acting as leading role in planning, coordinating, and completing project work
    • Work closely with the internal and external stakeholders, such as internal project team members, vendors, and suppliers to ensure success in assigned projects.
    • Management of deliverables and timelines
    • Bid defences, pitching to external pharma and biotech
    • Budgeting and change order responsibilities

    Requirements:

    • Full-service project management experience.
    • Several years Project Management experience within a CRO.
    • International experience managing global projects.

    This Clinical Project Manager role is a home-based role in Germany. It is a permanent role offering around €60K-€75K+ bonus + benefits.

    Skills Alliance are the exclusive partner for this role. Please contact Filip Szurkiewicz for more details on +44 203 910 1229 or click APPLY NOW.

  • Clinical Operations

    €75000 - €90000 per annum, + benefits + bonus
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    Job
    Application

    You are currently registered and logged onto our site and this form is therefore using the personal details and CV you have saved with your profile. You can amend them here but they won't overwrite your saved account details. The new uploaded CV and/or cover letter will be saved onto your account if it is not exceeding the maximum of 5 documents.

    Before applying for this position you need to submit your online CV. Click the button below to continue.


    Share

    Senior Clinical Project Manager – Home based in Europe
    A US based, Global CRO, specialising in the generation, analysis and communication of real-world evidence throughout the product lifecycle.
    This is a great opportunity to join a rapidly growing SME CRO, with major developments coming within the EU in recent years, following its re-establishment as a standalone provider of pharmaceutical services. With this expansion, there are great opportunities for professional development and progression. They work within evidence-based research with a primary focus on rare disease, novel indications, and speciality therapies.
    Responsibilities:

    • Operational oversight of projects, acting as leading role in planning, coordinating, and completing project work
    • Work closely with the internal and external stakeholders, such as internal project team members, vendors, and suppliers to ensure success in assigned projects.
    • Management of deliverables and timelines
    • Bid defences, pitching to external pharma and biotech
    • Budgeting and change order responsibilities

    Requirements:

    • Full-service project management experience.
    • Several years Project Management experience within a CRO.
    • International experience managing global projects.

    This Senior Clinical Project Manager role is a home-based role in Germany. It is a permanent role offering around €75K-€90K+ bonus + benefits.

    Skills Alliance are the exclusive partner for this role. Please contact Filip Szurkiewicz for more details on +44 203 910 1229 or click APPLY NOW.

  • Clinical Operations

    €75000 - €90000 per annum, + benefits + bonus
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    Job
    Application

    You are currently registered and logged onto our site and this form is therefore using the personal details and CV you have saved with your profile. You can amend them here but they won't overwrite your saved account details. The new uploaded CV and/or cover letter will be saved onto your account if it is not exceeding the maximum of 5 documents.

    Before applying for this position you need to submit your online CV. Click the button below to continue.


    Share

    Senior Clinical Project Manager – Home based in Europe
    A US based, Global CRO, specialising in the generation, analysis and communication of real-world evidence throughout the product lifecycle.
    This is a great opportunity to join a rapidly growing SME CRO, with major developments coming within the EU in recent years, following its re-establishment as a standalone provider of pharmaceutical services. With this expansion, there are great opportunities for professional development and progression. They work within evidence-based research with a primary focus on rare disease, novel indications, and speciality therapies.
    Responsibilities:

    • Operational oversight of projects, acting as leading role in planning, coordinating, and completing project work
    • Work closely with the internal and external stakeholders, such as internal project team members, vendors, and suppliers to ensure success in assigned projects.
    • Management of deliverables and timelines
    • Bid defences, pitching to external pharma and biotech
    • Budgeting and change order responsibilities

    Requirements:

    • Full-service project management experience.
    • Several years Project Management experience within a CRO.
    • International experience managing global projects.

    This Senior Clinical Project Manager role is a home-based role in Netherlands. It is a permanent role offering around €75K-€90K+ bonus + benefits.

    Skills Alliance are the exclusive partner for this role. Please contact Filip Szurkiewicz for more details on +44 203 910 1229 or click APPLY NOW.

  • Clinical Operations

    €75000 - €90000 per annum, + benefits + bonus
    Apply

    Job
    Application

    You are currently registered and logged onto our site and this form is therefore using the personal details and CV you have saved with your profile. You can amend them here but they won't overwrite your saved account details. The new uploaded CV and/or cover letter will be saved onto your account if it is not exceeding the maximum of 5 documents.

    Before applying for this position you need to submit your online CV. Click the button below to continue.


    Share

    Clinical Project Manager – Home based in Europe
    A US based, Global CRO, specialising in the generation, analysis and communication of real-world evidence throughout the product lifecycle.
    This is a great opportunity to join a rapidly growing SME CRO, with major developments coming within the EU in recent years, following its re-establishment as a standalone provider of pharmaceutical services. With this expansion, there are great opportunities for professional development and progression. They work within evidence-based research with a primary focus on rare disease, novel indications, and speciality therapies.
    Responsibilities:

    • Operational oversight of projects, acting as leading role in planning, coordinating, and completing project work
    • Work closely with the internal and external stakeholders, such as internal project team members, vendors, and suppliers to ensure success in assigned projects.
    • Management of deliverables and timelines
    • Bid defences, pitching to external pharma and biotech
    • Budgeting and change order responsibilities

    Requirements:

    • Full-service project management experience.
    • Several years Project Management experience within a CRO.
    • International experience managing global projects.

    This Clinical Project Manager role is a home-based role in Netherlands. It is a permanent role offering around €75K-€90K+ bonus + benefits.

    Skills Alliance are the exclusive partner for this role. Please contact Filip Szurkiewicz for more details on +44 203 910 1229 or click APPLY NOW.

  • Commercial

    €50000 - €60000 per annum, company car, phone, computer
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    Job
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    Before applying for this position you need to submit your online CV. Click the button below to continue.


    Share

    AUFGABEN
    Der Account Manager bewirbt und verkauft die gesamte Produktpalette, einschließlich Instrumente, Pipetten, Verbrauchsmaterialien und Dienstleistungen in dem zugewiesenen Gebiet, um die budgetierten Verkaufsziele zu erreichen. Um diese Ziele zu erreichen, wendet er die besten Verkaufspraktiken an und fördert ein gesundes, nachhaltiges Gebiet durch Konzentration auf Kundenbindung, -entwicklung, -durchdringung und anhaltende Zufriedenheit. Nutzt eine Multi-Channel-Umgebung zur Maximierung des Umsatzes unter Verwendung von Distributoren- und Händler Beziehungen. Hat direkten Einfluss auf die Mission, verifizierbare Wissenschaft zu ermöglichen, indem er Wissenschaftlern dabei hilft, die Produkte auszuwählen, die sie für ihre Arbeit am effektivsten benötigen.

    WESENTLICHE PFLICHTEN UND VERANTWORTLICHKEITEN

    · Erreicht oder übertrifft die festgelegten Ziele für Verkaufsvolumen, Produktmix und Bekanntheit neuer Produkte und Dienstleistungen im zugewiesenen Gebiet.
    · Treibt den MLH-Verkauf voran (Produkte einschließlich Pipetten, Tischgeräte, Verbrauchsmaterialien und Dienstleistungen); findet, qualifiziert und nutzt das CRM-System, um komplexe Instruments-Leads zu dokumentieren
    · Reist durch das Gebiet, um bestehende und potenzielle Kundenkontakte aufzusuchen, um die Nachfrage nach Produkten und -Dienstleistungen zu steigern. Zu den Aktivitäten gehören Produkteinführungen und -Überblicke, die Durchführung von Vorführungen, technischen Seminaren, Fehlersuche, die Teilnahme an lokalen und nationalen Messen und die Bereitstellung der notwendigen Nachbereitung und Entwicklung, um Produkt- und Serviceverkäufe zu erzielen. Organisiert Reisen, um eine maximale Kundenabdeckung bei gleichzeitiger Minimierung der Reisekosten zu gewährleisten.
    · Verfolgt und bearbeitet Verkaufskontakte auf der Grundlage von Informationen, die er von anderen -Vertriebsmitarbeitern, Firmenmessen, Marketingkampagnen, Telefon- und Website-Anfragen und anderen Quellen erhält.
    · Wendet die Verkaufstechniken und Best Practices von Gilson während des gesamten Verkaufszyklus an, um die Ziele zu erreichen.
    · Übermittelt und pflegt genaue monatliche Prognosen über das Opportunity Management in Salesforce.com.
    · Pflegt und aktualisiert Gebietsdaten für Kunden und Schlüsselpersonen in Salesforce.com (SFDC).
    · Arbeitet mit technischen Service-Ingenieuren und Anwendungsspezialisten im Bereich Instruments zusammen, um einen proaktiven Verkaufs-, Service- und Support-Ansatz innerhalb des zugewiesenen Gebiets zu fördern.
    · Erstellt Angebote und Preisvereinbarungen unter Einhaltung der Preisrichtlinien.
    · Nimmt an erforderlichen und empfohlenen Schulungen teil, um ein fundiertes technisches und anwendungstechnisches Wissen über das Gilson-Produktportfolio zu erlangen und zu erhalten.
    · Arbeitet mit dem Service- und Supportpersonal zusammen, um nach dem Verkauf Installationen, Schulungen und fortlaufenden Servicevertragssupport zu bieten, falls erforderlich.
    · Arbeitet bei Bedarf mit dem Corporate Accounts Team für alle Corporate Accounts im Gebiet zusammen.
    · Er schult, motiviert und arbeitet bei Bedarf mit Distributoren und Händlern zusammen und nutzt die Beziehungen zur weiteren Durchdringung von Schlüsselkunden.
    · Hält sich auf dem Laufenden über Trends und Aktivitäten im Gebiet, Wettbewerbsprodukte und -preise sowie Kundenanliegen in Bezug auf Gilson-Produkte, die vor Ort beobachtet werden, und informiert diese zeitnah.
    · Entwickelt und führt Zeitmanagement und Geschäftspläne für Accounts/Gebiete aus.
    · Andere Aufgaben wie zugewiesen.

    ARBEITSANFORDERUNGEN

    · AUSBILDUNG
    · Hochschulabschluss in Biowissenschaften oder einem verwandten wissenschaftlichen Bereich.
    · BERUFSERFAHRUNG
    · Mindestens 3 Jahre Vertriebserfahrung in einer verwandten Branche oder eine Kombination aus hochtechnischem Hintergrund und Vertriebserfahrung.

    FÄHIGKEITEN ODER WISSEN

    · Ausbildung in Laborwissenschaften und/oder Biowissenschaften.
    · Computerkenntnisse erforderlich.
    · Begabung im technischen Bereich.
    · CRM Erfahrungen für den täglichen Gebrauch zur Einpflege von Daten
    · Fähigkeit zum Lesen, Analysieren und Interpretieren von allgemeinen Geschäftszeitschriften, Fachzeitschriften, technischen Verfahren oder behördlichen Vorschriften.
    · Fähigkeit, Geschäftskorrespondenz und Berichte zu schreiben. Fähigkeit, Informationen effektiv zu präsentieren und auf Fragen von Kunden, Händlern und Firmenpersonal zu antworten.
    · Fähigkeit, Zahlen und Beträge zu berechnen, z. B. Rabatte, Prozentsätze und Volumen.
    · Fähigkeit, technische Probleme zu lösen und mit einer Vielzahl von Variablen umzugehen.
    · Ausgeprägte organisatorische Fähigkeiten.
    · Umfassende Verkaufsfähigkeiten und -techniken einschließlich Verhandlungsführung.
    · Fließende Beherrschung der deutschen Sprache, Kenntnisse in englischer Sprache erforderlich.

    SONSTIGES

    · Ein gültiger Führerschein und eine gute Fahrpraxis und sind erforderlich.
    · Bis zu 60 % Reisetätigkeit einschließlich Übernachtungen.
    · Regelmäßige Anwesenheit und Pünktlichkeit.
    · Fähigkeit, gut mit Anderen zusammenzuarbeiten.
    · Fähigkeit, sich neue Fähigkeiten anzueignen und sich auf Veränderungen am Arbeitsplatz einzustellen.

    ZUSÄTZLICHE FÄHIGKEITEN/ERFAHRUNGEN VON VORTEIL
    ·
    · Ausbildung oder Erfahrung im Umgang mit Labor- oder Forschungsinstrumenten.
    · Erfahrung im Umgang mit -Pipetten und -Instrumenten.
    · Ausbildung in analytischer oder organischer Chemie.
    · Erfahrung im Verkauf von Investitionsgütern.

  • Sales & Marketing

    €40000 - €45000 per annum, bonus
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    On behalf of our customer, we are looking for an enthusiastic Inside Sales Rep to achieve our customer acquisition and sales growth goals. Be familiar making calls, working with sales associates, generating interest, qualifying prospects and closing sales.

    1x Customer Area: Bavaria/Austria
    1x Customer Area: Switzerland

    Responsibilities
    Develop new sales opportunities through inbound lead follow up and outbound cold calls and emails.
    Understanding customer needs and requirements
    Closing sales and achieving revenue targets
    Researching customers, identifying key people and generating interest
    Maintaining and expanding database of potential customers in assigned territory
    Working with channel partners to build pipelines and close deals
    Conduct effective online demos for potential clients

    Requirements

    • Degree in Life Sciences or related scientific field- Cell and molecular biology would be an advantage
    • experience in sales/inside sales of Manual and Automatic Liquid Handling (MLH/HPLC/SPE)
    • Strong phone presence and experience making on calls
    • listening and presentation skills Ability to prioritize and manage time effectively
    • Good computer skills (MS-Office, marketing tools) Strong
    • Experience working with CRM system, experience with Salesforce.com an advantage
    • Excellent written and verbal communication skills
    • Business fluent in German and very good written and spoken English and French ( only for one open position)
    • Flexibility and enthusiasm
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    For our client in Zurich, we are looking for a Sr. Manager Regulatory Affairs for a 6.5 months contract.

    OBJECTIVE:
    • Under supervision from a senior team member and/or Line Manager defines, develops and sometimes leads regional strategies to maximize regulatory approvals and patient access to meaningful medicines in alignment with program objectives
    • Effectively communicates objective assessments of the likelihood of success of these regulatory strategies
    • Provides regional strategic and tactical advice and guidance to teams to achieve timely and efficient conduct of development programs, while maintaining full compliance with applicable regulatory requirements
    • Leads the Regional Working Team and represents the region as needed on global and project teams
    • Provides regional regulatory expertise for assigned development and /or life cycle management projects within the therapeutic area of responsibility
    • Under supervision from a senior team member and/or Line Manager sometimes manages interactions with EMA and national health authorities (and HTAs in context of parallel consultation) in the European Region for product(s) within their responsibility.

    ACCOUNTABILITIES:
    • Ensures regional regulatory strategies are written, reviewed and executed according to plan
    • In alignment with line manager, provides strategic and tactical advice and guidance to allow the timely and efficient conduct of development programs, while maintaining full compliance with applicable regulatory requirements
    • Manages, plans, and executes regional regulatory submissions within the area of responsibility and ensures timely approvals throughout product development and lifecycle
    • Partners with the regional market access and LOC RA colleagues to define the strategy for, and to lead and oversee joint interactions with regional and national regulatory/health agency/HTA bodies on value and evidence topics and to support heath authority decision making
    • Collaborates with Global and Regional counterparts and Integrated Franchise Team (IFT) to ensure the regional regulatory strategy is created and executed upon for all projects within area of responsibility
    • Identifies relevant regional regulatory requirements and trends across scope of responsibility, and provides regulatory guidance, and expertise to global development team and/or higher governance bodies in these areas
    • Monitors and informs on emerging trends, regulations and changes, with emphasis on those related to area and region of responsibility
    • May be called upon to provide direction to senior leadership, as relevant
    • Develops and maintains effective working relationships with RA and Rare Genetic & Hematology Team members, LOC RA teams, Global Regulatory Teams, Cross-functional Teams; consultants and business partners as required
    • Oversees and accountable for working with other RA functions and/or vendor to ensure that regulatory submissions and approvals are achieved on schedule within area of responsibility
    • Understands importance of regulatory documents for value and access discussions and partners with access functions to support access applications as needed
    • In collaboration with global colleagues, works to resolve regional critical conflicts in global regulatory strategies.
    • Authors and oversees execution for more complex regional regulatory strategies as needed
    • Under supervision from a senior team member and/or Line Manager, sometimes leads and manages meetings and / or interactions with regulatory authorities and agency meetings; in alignment with line manager can negotiate on behalf of project team as necessary.
    • Under supervision from a senior team member and/or Line Manager, sometimes represents the company in Health Authority meetings, as required. Effectively communicates and manages meeting outcome and next steps
    • May be required to lead and provide regional regulatory input in due diligence for licensing opportunities, development and /or marketed products
    • Pro-actively builds/strengthens external stakeholder (Regulatory Agency, external experts, industry organizations, etc) contacts/influence to support Takeda strategic goals and objectives
    • Identifies regulatory requirements across area(s) of responsibility, and provides regulatory guidance, and expertise to global development team and /or higher governance bodies in these areas
    • Ensures coverage for projects within the therapeutic area identifies possible gaps, and proposes solutions to the management
    • Presents regional regulatory strategies to senior management as applicable

    EDUCATION, BEHAVIOURAL COMPETENCIES AND SKILLS:
    • BSc. Advanced scientific related degree preferred; BA accepted based on experience. Advanced degree preferred
    • Considerable experience within the pharmaceutical industry and including direct experience in regulatory affairs in development and /or post-marketing phases.
    • Solid working knowledge of regulations and guidelines governing drugs and biologics in development, including post-marketing in the EU
    • Understands and interprets complex scientific issues across projects and therapeutic area(s) of responsibility as it relates to regulatory requirements and strategy
    • Preferred experience in managing multiple filings; or managing multiple programs in closely related development area; expertise in the EU region (as relevant to role) with global involvement also preferred
    • Generally strong in all basic skills sets such as oral and written communications, managing and adhering to timelines, negotiation skills, integrity and adaptability
    • Able to understand broad concepts within regulatory affairs and implications across the organization and globally
    • Proactively identifies regulatory issues; offers creative solutions and strategies, including risk mitigation strategies.
    • Generally strong in working well with others, within global teams and communicating with senior leadership.
    • Takes stand on important issues in productive, respectful way.
    • Experience managing relationships with CROs and/or contractors also preferred.

    ADDITIONAL EUROPE SPECIFIC INFORMATION :

    • A minimum of 6 years of pharmaceutical industry experience. This is inclusive of 5 years of regulatory experience or combination of 6 years regulatory and/or related experience.

  • HR and talent acquisition

    £30000 - £35000 per annum
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    An exciting opportunity for an experienced Coordinator, looking for progression opportunities within Training.

    The Training Coordinator will be responsible for coordinating high volumes of training for a Pharmaceuticals manufacturing facility in Hertfordshire. This role sits within a small team of GMP (Good Manufacturing Practice) Trainers and there is an opportunity for you to progress towards delivering training yourself. The company will support your training and development to this level.

    In return, they are seeking a self-starter with some experience in a coordination role (not neccessarily in the training field). You must have the ability to think on your feet and use your own initiative.

    This is an initial 6-month contract that will turn into a permanent position afterwards.

    For more information, please contact Sarah Brambill at Skills Alliance.

  • Pre-Clinical

    £65000 - £78000 per annum, Bonus + benefits + shares
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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 is permanent and the office is based in Central London (with flexibility).

    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 and we have had great feedback from recent placements.

    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. It is a great opportunity to gain gene therapy/advanced therapies experience.

    This is a permanent and full-time role. The role would be home-based initially with travel to the Central London office. They offer an excellent salary – GBP 65,000-78,000 + bonus + benefits + shares.

    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

    Competitive
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    Skills Alliance is currently partnered with the leading global mid-sized CRO. For this purpose, our client is looking for a Clinical Research Associate (CRA) to join their team.

    All roles are Sponsor based- leading Global Pharma company.

    1) CRA Ophthalmology (Fully remote) Either to be based in Barcelona or Madrid: This involves national travel. At least 3 years of experience working as a CRA within therapeutic area Ophthalmology. Freelance CRA (minimum 0.4 FTE-0.5 FTE is needed – the client is also open for more FTE.

    2) Jr. CRA (office based) : Permanent role: To be based in Madrid Spain: involves national travel; Atleast 6 months of experience as a CRA.

    3) CRA (partial remote: To be based in Barcelona: Permanent Role: involves regional travel. Atleast 1 year of working as a CRA independently.

    4) CRA: Fully remote: to be Based in Galicia, Spain: Permanent Role: involves regional travel. Atleast 1 year of working as a CRA independently.

    If interested or you know someone who would be interested please apply directly here or email at heena.verma@skillsalliance.com or phone @ +41 44 798 2410.

    Thanks!

    Best,
    Heena Verma
    Recruitment Consultant, Europe | Clinical Operations | Zürich

  • Clinical Operations

    Competitive
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    Skills Alliance is currently partnered with the leading global mid-sized CRO. For this purpose, our client is looking for a Clinical Research Associate (CRA) to join their team on a permanent role.

    This role is to be based in Milan, Italy.

    2 roles:

    1) You have to be based in Milan, Italy: CRA Junior: This involves national travel. At least 6 months of experience working as a CRA (with certificate)

    2) Fully remote: You can be based anywhere in Lombardy region: CRA Oncology: (national travel) – At least 18 months of experience working as a CRA (with certificate, involved in some oncology studies). Our client is considering candidates who are even with other therapeutic area but with some experience within oncology.

    If interested or you know someone who would be interested please apply directly here or email at heena.verma@skillsalliance.com or phone @ +41 44 798 2410.

    Thanks!

    Best,
    Heena Verma
    Recruitment Consultant, Europe | Clinical Operations | Zürich

  • Clinical Operations

    Competitive
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    Skills Alliance is currently partnered with the leading global mid-sized CRO. For this purpose, our client is looking for a Clinical project Manager to join their team on a permanent role.

    This role can either be based in Barcelona or Madrid.

    RESPONSABILITIES:

    • Active participation in the preparation of Clinical Development plans
    • Collaboration in the elaboration and review of clinical trials outlines, DSUR, IB, and international (Europe/FDA) submission dossiers.
    • Participation and reporting to the Project Team (PT), Medical Sub Team (MST), Core Teams and, any other team as needed.
    • Participation in advisors, partners or in- and out-licences meetings, including the preparation and review of associated documentation.
    • Collaborate in the creation of presentations for congresses and/or papers for medical journals based on CT results.
    • Planning and conduct of clinical trials/experimental and cosmetic testing/investigations with medical devices, including preparation, review or approval of all associated documentation (synopsis, protocol, report, timelines, all study plans –statistical, data management, monitoring,…-, technical specifications, IMP related documents, and any other study-related documentation) and management of study budget, including approval of invoices payment and forecast planning.
    • CRO and other vendors selection for the outsourcing of Clinical Trials and other activities task according to Project needs.
    • Leadership and coordination of the different areas and activities of the “Clinical Study Team.
    • Cooperation with other department representatives when needed: Global Sourcing, Pharmacokinetics and Metabolism, Biology, Pharmacology, Regulatory Affairs, Marketing, GMA-MA, Corporate Global Drug Safety, Pharmaceuticals, Affiliates, Intellectual Property, Quality Assurance, Global Clinical Leader and Global Safety Leader.
    • Participate in the preparation of any documentation related to competent national and local authorities, and the relevant ethics committees, coordinate and boost regulatory submissions and answer to their questions.
    • Organize and/or participate in the Investigators Meeting/Pre-initiation visits/Kick-off Meetings presenting the protocol and study operational aspects (study drug, monitoring) of the study, and visit research sites ad-hoc
    • Supervise and boost sites activation and recruitment progress, database cleaning, and timely SAE reporting.
    • Review of the Trial Master File key documents related to activities under CTM direct responsibility.
    • Collaboration in the planning and conduction of audits and CAPA implementation, and in the inspections to the participating sites or sponsor.
    • Ongoing review of CT blinded data (e.g. for identification of protocol deviations, ensuring accuracy of data cleaning, early detection of unexpected trends on patients baseline characteristics).
    • Leadership of the “Blind Data Review Meeting”.
    • Ensuring the CT are conducted in accordance with Good Clinical Practices (GCPs), with applicable international quality standards, with the agreed SOPs, policies and standards, as well as any other guidelines given by the Head of Global Clinical Operations (GCO) and GCL.
    • Report and discuss with the Medical sub team Escalation to the GCL and/or Project Manager and Head of GCO any significant deviation (or a risk for deviation) from the agreed timelines, budget, qualitative metrics or standards at any time during the trial.
    • Continuing education and training on medical and clinical research topics, national and international policies for the development of CT.
    • Collaboration in SOPs update/creation/training.


    REQUIREMENTS

    Diploma in Nursing and/or Graduate in Health Sciences (Pharmacy, Biology, Biochemistry and/or Medicine and Surgery).

    · Participation in Clinical Trials
    · Must have experience within clinical studies from site initiation until close-out
    · Pharmaceutical Industry business
    · Project Management
    · Basic Statistics and/or Biometry
    · Basic Pharmacokinetics, Clinical Toxicology and Pharmacology
    · Others: Preferably Doctor’s degree
    · English essential (Other languages desirable)

    If interested or you know someone who would be interested please apply directly here or email at heena.verma@skillsalliance.com or phone @ +41 44 798 2410.

    Thanks!

    Best,
    Heena Verma
    Recruitment Consultant, Europe | Clinical Operations | Zürich

  • Medical affairs

    Competitive
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    Skills Alliance is currently partnered with the leading global mid-sized CRO based in Madrid. For this purpose, our client is looking for a Medical Specialist to join their team on a permanent role.

    FUNCTIONS:

    – Coordination of the development of projects from a scientific and clinical point of view.
    – Design and maintenance of the protocols of the studies sponsored by the assigned company, as well as review of their design and execution in their scientific, clinical and methodological aspects.
    – Preparation of the clinical section of documents required in clinical research (Informed Consents, Investigator’s Manuals, Aggregate Reports, etc.
    – Review and analysis of clinical trial data from the clinical point of view and its reporting in the final reports.
    – Participation in the selection of centres and investigators participating in clinical trials.
    – Medical responsible for the protocols under his/her responsibility, providing the necessary clinical support for their correct follow-up.
    – Collaboration in the communication of results in scientific publications and congresses.
    – Support to the Regulatory Affairs Area in the documentation related to the marketed product from a scientific point of view and to the Marketing and Business Development Department.

    REQUIREMENTS:

    – Degree in Medicine
    – High level of English (other languages are a plus)
    – At least 2 years’ experience in similar positions or in other positions within Medical Affairs and/or Clinical Research departments is desirable.

    If interested or you know someone who would be interested please apply directly here or email at heena.verma@skillsalliance.com or phone @ +41 44 798 2410.

    Thanks!

    Best,

    Heena Verma
    Recruitment Consultant, Europe | Clinical Operations | Zürich

  • Clinical Operations

    $95000 - $135000 per annum
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    Share

    I am working on a unique opportunity to join a pioneering and well-established research facility.

    I am working with a US based company specialising in paediatric Oncology, ranking in the top 5 paediatric research centres in America. They have numerous ground-breaking treatments ranging from Cystic Fibrosis to immuno-oncology therapies.
    I am supporting the recruitment of a CTM 2 and a Senior CTM, hiring across Seattle, Georgia, Texas and Florida.

    The Trial Manager will be responsible for full oversight of single and multi-site clinical trials, guaranteeing the research projects are carried out in compliance with applicable federal and local regulations. Management and mentoring of clinical sites, resources, and vendor(s) as applicable.

    The right candidate must demonstrate experience in leading teams in a matrixed environment, with in depth knowledge of trial management, developing study material (protocols, plans, manuals) and evaluating site performance against established criteria. Phase 1 & 2 clinical research experience is also required. A good understanding of oncology is strongly preferred.

  • Medical Devices

    €35000 - €55000 per annum
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    An international innovative medical device company is looking for a FSE (Field Service Engineer) anywhere in Spain.

    A ground-breaking medical system is used successfully in the operating room and needs to be supported by a professional across the country.

    The Field Service Engineer should ideally be located within 1 hour drive to an international airport.

    Main tasks: installation, technical support, troubleshooting and maintenance of the medical device in surgical room.

    Travelling: around 80% of the time

    Must have: an experience in field tech. support (preferably medical area), English & Spanish

    Advantage: an experience with medical capital equipment

    If you speak English and can work in English, want to travel a lot and be a part of an international team, I would be happy to share with you the detailed job description and have a call for more details. Kindly contact me at T: 0041 43 508 69 62 or E: maria.nosach@skillsalliance.com

    Best regards,
    Maria Nosach

  • Regulatory

    €80000 - €100000 per annum, Attraktives Gesamtpaket mit guter Altersvorsorge und sonstigen guten Sozialleistungen
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    Unser Kunde, ein interationales Biotec Unternehmen, ist auf der Suche nach einem erfahrenen “Regulatory Affairs Manager” in Festanstellung. Wenn Sie die folgenden Aufgaben ansprechen, freuen wir uns sehr auf Ihre Bewerbung:

    • Sie bringen langjähre Zulassungserfahrung in der pharmazeutischen bzw Biotec Industrie mit
    • Die Zusammenarbeit mit den relevanten Zulassungsbehörden ist Ihnen bestens vertraut
    • Sowohl die Dossierarbeit als auch die Arbeit im CCDS liegt Ihnen und bereitet Ihnen auch zukünftig Freude
    • Sie arbeiten eng mit den Bereichen Pharmakovigilanz und Drug Safety zusammengearbeitet

    Ihre Qualifikation:

    • Sie haben Ihr Studium im Bereich Pharmzie o.ä. erfolgreich abgeschlossen
    • Sie bringen einschlägige Berufserfahrung in der pharmazeutischen bzw. Biotec Industrie mit
    • Sie bringen sehr gute Deutsch und Englischkenntnisse mit (schriftlich & mündlich)
  • Clinical Operations

    $95000 - $135000 per annum
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    Share

    I am working on a unique opportunity to join a pioneering and well-established research facility.

    I am working with a US based company specialising in paediatric Oncology, ranking in the top 5 paediatric research centres in America. They have numerous ground-breaking treatments ranging from Cystic Fibrosis to immuno-oncology therapies.
    I am supporting the recruitment of a CTM 2 and a Senior CTM, hiring across Seattle, Georgia, Texas and Florida.

    The Trial Manager will be responsible for full oversight of single and multi-site clinical trials, guaranteeing the research projects are carried out in compliance with applicable federal and local regulations. Management and mentoring of clinical sites, resources, and vendor(s) as applicable.

    The right candidate must demonstrate experience in leading teams in a matrixed environment, with in depth knowledge of trial management, developing study material (protocols, plans, manuals) and evaluating site performance against established criteria. Phase 1 & 2 clinical research experience is also required. A good understanding of oncology is strongly preferred.

  • Clinical Operations

    $95000 - $135000 per annum
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    Before applying for this position you need to submit your online CV. Click the button below to continue.


    Share

    I am working on a unique opportunity to join a pioneering and well-established research facility.

    I am working with a US based company specialising in paediatric Oncology, ranking in the top 5 paediatric research centres in America. They have numerous ground-breaking treatments ranging from Cystic Fibrosis to immuno-oncology therapies.
    I am supporting the recruitment of a CTM 2 and a Senior CTM, hiring across Seattle, Georgia, Texas and Florida.

    The Trial Manager will be responsible for full oversight of single and multi-site clinical trials, guaranteeing the research projects are carried out in compliance with applicable federal and local regulations. Management and mentoring of clinical sites, resources, and vendor(s) as applicable.

    The right candidate must demonstrate experience in leading teams in a matrixed environment, with in depth knowledge of trial management, developing study material (protocols, plans, manuals) and evaluating site performance against established criteria. Phase 1 & 2 clinical research experience is also required. A good understanding of oncology is strongly preferred.

  • Clinical Operations

    $95000 - $135000 per annum
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    Before applying for this position you need to submit your online CV. Click the button below to continue.


    Share

    I am working on a unique opportunity to join a pioneering and well-established research facility.

    I am working with a US based company specialising in paediatric Oncology, ranking in the top 5 paediatric research centres in America. They have numerous ground-breaking treatments ranging from Cystic Fibrosis to immuno-oncology therapies.
    I am supporting the recruitment of a CTM 2 and a Senior CTM, hiring across Seattle, Georgia, Texas and Florida.

    The Trial Manager will be responsible for full oversight of single and multi-site clinical trials, guaranteeing the research projects are carried out in compliance with applicable federal and local regulations. Management and mentoring of clinical sites, resources, and vendor(s) as applicable.

    The right candidate must demonstrate experience in leading teams in a matrixed environment, with in depth knowledge of trial management, developing study material (protocols, plans, manuals) and evaluating site performance against established criteria. Phase 1 & 2 clinical research experience is also required. A good understanding of oncology is strongly preferred.

  • Clinical Operations

    £60000 - £78000 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

    £65000 - £75000 per annum, Excellent package
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    Senior Global Clinical Study Manager position – purely working in Oncology, could be solid tumours or haematology. Study responsibility and line management of a small team.

    This is a great opportunity to join a reputable Biopharmaceutical company with a great reputation, they have a great pipeline spanning phase I-III and trials being run globally. They are growing and will offer excellent long-term opportunities. They are investing a huge amount in Oncology at present and we have had excellent feedback from recent placements.

    They are recruiting for a Senior Clinical Study Manager / Senior Global Trial Manager 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, with Oncology trial management and line management experience. They want someone who can work at a senior level and take on a leadership role in the team. It could be haematology or solid tumours.

    The role is full-time, permanent and home-based initially, office-based (2 days) with flexibility when things return to normal in London. They will offer an excellent salary and package – around £65-75K basic salary + excellent bonus + benefits + stock.

    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 - £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 Development

    £60000 - £80000 per annum, Bonus + benefits
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    *PHARMA EXPERIENCE REQUIRED*

    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 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 60-80K + 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.

  • Pre-Clinical

    £60000 - £80000 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 60-80K + 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

    £80000 - £95000 per annum, Excellent package
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    Senior Clin Ops role with an Oncology focussed Biopharma in London. Working at program level and leading their leading programs and line managing a small team.

    This is a rare opportunity to join a reputable Biopharmaceutical company with a great reputation, 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, with Oncology trial management and line management experience. They want someone who can work at a senior level and take on a leadership role in the team. It could be haematology or solid tumours.

    The role is full-time, permanent and home-based initially, office-based (2 days) with flexibility when things return to normal in London. They will offer an excellent salary and package – around £80-905K basic salary + bonus + benefits + stock.

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

  • HR and talent acquisition

    Competitive
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    A rapidly growing Biopharmaceuticals company in Hertfordshire is seeking a Talent Acquisition Business Partner to join their small and friendly team.

    They are seeking:
    – An experienced Talent Acquisition / Internal Recruitment Specialist
    – Ability to work independently in a fast-paced environment
    – Experience working closely with hiring managers
    – Confident with high volume manufacturing recruitment
    – Life Sciences of FMCG background

    They are offering:
    – Opportunity to work within a highly regarded therapeutic area and rapidly growing company
    – Initial contract offering a competitive rate of pay – opportunity to move to permanent employment in 2022
    – Small, highly experienced team
    – Opportunity for progression and more responsibility as the company grows

    Please contact Sarah Brambill from Skills Alliance to discuss this opportunity in further detail.

  • Project Management

    £60000 - £78000 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

    £75000 - £95000 per annum, Excellent package
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    Global Clinical Program Manager position – purely working in Advanced therapies Oncology. Study responsibility and line management of a small team.

    This is a great opportunity to join a World-class Biopharmaceutical company with a strong reputation, they have a great pipeline spanning phase I-III and trials being run globally. They are growing and will offer excellent long-term opportunities. They are investing a huge amount in Oncology at present and we have had excellent feedback from recent placements.

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

    The role is full-time, permanent and home-based initially, office-based (2 days) with flexibility when things return to normal in the London area. They will offer an excellent salary and package – around £75-95K basic salary + excellent bonus + benefits + stock.

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

  • Clinical Operations

    $135000 - $170000 per annum, + 20% profit share scheme
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    I have a rare opportunity within a small and niche company who are currently growing in the US.

    They have a focus in Oncology, Immunology, Rare and Neurodegenerative diseases. They have achieved over 50 market authorizations to date. Since their inception in 2004, they pride themselves on providing a highly individualised service for their clients, because of this, they have seen consistent growth across the globe. Using first-in-class technology platforms alongside relationship driven flexibility ensures a high level of service. There are office locations globally, spanning across North America, the UK, Europe and Australia.

    I am working to hire a Senior/AD Project Manager role with a strong focus on external facing business development. This role will be directly involved with the senior management of the company, involved in strategic decision making with the growth and development of the company in mind. The right candidate will display complete proficiency in all aspects of full-service Project Management in Phases I through IV in Oncology, with a preference for candidates with experience in any of: immunology, neurology, CAR-T or gene therapy.

    The role offers home working flexibility, with a minimal need for travel, only travelling when necessary. As such, this role is open to candidates across the whole of the US. The role reports directly into VP level.

    You can expect a salary range from $135k-$170k with an excellent benefits package. There is a big emphasis on a healthy work life balance, providing flexibility with PTO.

    Do you know anyone who would be open to discuss further details?

  • Clinical Operations

    £45000 - £55000 per annum, + company profit share, depending on levels of experience + benefits
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    I have a rare opportunity within a small and niche company who are currently growing in the UK.

    They have a focus in Oncology, Immunology, Rare and Neurodegenerative diseases. Theyhave achieved over 50 market authorizations to date. Since their inception in 2004, they pride themselves on providing a highly individualised service for their clients, because of this, they have seen consistent growth across the globe. Using first-in-class technology platforms alongside relationship driven flexibility ensures a high level of service.

    There are office locations globally, spanning across North America, the UK, Europe and Australia. They are looking for an experienced CRA to join the team at either CRA II or Senior CRA level, it is a wide ranging role working closely with the senior management (including CEO) so great exposure and you would be one of two CRAs in the UK with around 7 site visits on average per month.

    The main focus in the initial stages of the role will be looking Infectious Diseases but they have Oncology projects coming up too. They are big on work/life balance and offering great support to their staff, hence they have very low turnover.

    This is a permanent and full-time position, offering full time working from home, with the exception of site visits as mentioned above. They also have an office in the South East. You can expect a salary ranging between £45,000-£55,000 + company profit share, depending on levels of experience + benefits. They would like someone to start in January ideally, or sooner.

    Would you be keen to discuss this role further? Or can you recommend anyone, if not?

  • Medical affairs

    €100000 per annum, attraktives Bonuspaket, gute Altersvorsorge,
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    Wir suchen aktuell für einen unserer Kunden, ein internationales und wachsendes Biotech Unternehmen, auf der Suche nach Verstärkung für das MSL Team im Bereich der Onkologie.

    Das sind Ihre Aufgaben:

    • Aufbau und Indentifikation aber auch vor allem Weiterentwicklung von Experten und medizinsichen-wissenschaftlichen Zentren
    • Aufbau eines stabilen Netzwerks an KOLs im Indikationsgebiet Onkologie
    • Enge Zusammenarbeit mit den wissenschaftlichen Abteilungen innerhalb des Unternehmens
    • Teilnahme und Organisation von internationalen und nationales Kongressen, Symposien und AdBoards
    • Unterstützung bei internen und exterenen Studienprojekten

    Das bringen Sie mit:

    • Abgeschlossenes naturwissenschaftliches Studium im Bereich Pharmazie, Chemie, Biologie
    • Optimalerweise bringen Sie bereits Erfahrung als MSL in der Onkologie mit und sind auf der Suche nach dem nächsten Schritt
    • Sie arbeiten gerne in crossfunktionalen Teams
    • Sie bringen sehr gute Gesprächs-/ und Kommunikationsfähigkeiten in deutscher und englischer Sprache mit
  • Clinical Operations

    £60000 - £80000 per annum, excellent package
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    A rare opportunity to join a growing early stage Biotech as they build their clinical team. This is a permanent Senior Clinical Study Manager role, mainly home-based with a little travel to the office – Cambs/Herts.

    This exciting and innovative Biotech company are at early stages with trials and just progressing into the clinic. 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 in phase I initially. They require substantial clinical trial management experience, ideally experience in early phase, complex TAs and ideally Biotech experience and/or the ability to work in a fast-paced and ambiguous environment.

    This is a full-time and permanent position. It is mainly home based – going to the office a few days per week. They offer an excellent salary and package around GBP 60-80K 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.

  • Quality

    Competitive
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    Möchten Sie ein wenig frischen Wind in Ihre Karriere bringen? Derzeit ist ein modernes Unternehmen mit Standort in Darmstadt, welches im Bereich Pharma/Biotech tätig ist, auf der Suche nach einem Quality Assurance Manager (m/w/d).

    Ihre Aufgaben sind:

    • Mitarbeit bei der Aufrechterhaltung, Überwachung und Weiterentwicklung des Qualitätsmanagement – Systems
    • Erstellung, Review, Verwaltung und Archivierung von lokalen Qualitätsdokumenten
    • Bearbeitung weiterer qualitätssichernder Prozesse
    • Ansprechpartner für qualitätsbezogene Fragestellungen
    • Mitwirken bei der Bearbeitung von Kunden- und Marktreklamationen
    • Sicherstellen der termingerechten Durchführung und Dokumentation von Qualitätsprüfungen

    Folgende Qualifikationen treffen auf Sie zu:

    • Pharmazeutische, naturwissenschaftliche Ausbildung oder ein abgeschlossenes Studium (z.B. Pharmazie, Biologie, Biochemie, Chemie, Medizin oder Naturwissenschaften)
    • Einschlägige Berufserfahrung im Bereich Qualitätssicherung
    • Gute konzeptionell analytische Denk- und Arbeitsweise
    • Ausgeprägte Kommunikationsstärke
    • Selbstständige, eigenverantwortliche und sorgfältige Arbeitsweise
    • Sehr gute Englischkenntnisse in Wort und Schrift

    Falls Ihr Interesse geweckt wurde, zögern Sie nicht uns zu kontaktieren!

  • HR and talent acquisition

    £45000 - £55000 per annum
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    A leading Pharmaceuticals company is seeking a Talent Acquisition specialist to report into their UK head office. The internal recruitment partner will be responsible for building talent pipelines throughout Europe and is required to have fluent German-language skills.

    In return, this forward-thinking organisation offers an entrepreneurial environment where innovation and creative thinking is highly rewarded. They offer an array of employee benefits including reduced working hours, full-time remote working available, annual bonuses and incentives.

    Responsibilities include:

    • Direct sourcing of candidates for vacancies from junior to senior executive level
    • Talent pipelining throughout europe
    • Building employer brand within the market place
    • Contribution to the overall growth and development of the talent acquisition function
    • Partners with the wider business and hiring manager to understand recruitment needs
    • Contributes ideas and uses initiative to work independently

    Requirements:

    • Life Sciences recruitment experience
    • German language skills
    • Accountable and pro-active in their approach to their work

    Please contact Sarah Brambill on 0207 220 6218 or sarah.brambill@skillalliance.com for more information about this opportunity or apply NOW for immediate consideration.

  • Regulatory

    €80000 - €100000 per annum, Gute Sozialleistungen und Altersvorsorge
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    Unser Kunde, ein internationales Biotec Unternehmen, ist auf der Suche nach einem erfahrenen „Regulatory Affairs Manager“ im Rhein-Neckar Gebiet. Es handelt sich hierbei um eine Festanstellung und bietet anderweitig sehr ansprechende Konditionen. Wenn Sie die folgenden Aufgaben ansprechen, freuen wir uns sehr auf Ihre Bewerbung:

    • Die Zusammenarbeit mit den Zulassungsbehörden fällt Ihnen leicht und ist Ihnen bestens vertraut
    • Sowohl die Dossierarbeit als auch die Arbeit im CCDS liegt Ihnen und bereitet Ihnen auch zukünftig Freude
    • Sie arbeiten eng mit den Bereichen Pharmakovigilanz und Drug Safety zusammen
    • Mithilfe bei der Durchführung von Audits
    • Erstellung von Produktzertifikaten und Administrationen der Zertifikatsdatenbank

    Ihre Qualifikationen:

    • Sie bringen langjährige Erfahrungen in der Zulassung für die Produkte der pharmazeutischen oder Biotec Industrie mit
    • Sie haben Ihr Studium im Bereich Pharmazie o.Ä. erfolgreich abgeschlossen
    • Sie bringen einschlägige Berufserfahrung in der pharmazeutischen oder Biotec Industrie mit
    • Sie bringen sehr gute (muttersprachliche) Kenntnisse in Deutsch, sowie sehr gute Kenntnisse in Englisch mit (in Wort und Schrift).

  • Clinical Operations

    $90000 - $125000 per annum
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    I am partnered with a World-class SME organisation at present to hire multiple Clinical Safety Manager roles – from Safety Manager II to Associate Director level.

    The company is dedicated to developing their employees in the long term, meaning there is a good opportunity to expand scope of responsibility (including line management if desired). Candidates will be expected to have displayed a stable career background, they have very low turnover, we have had excellent feedback from recent placements and they are a diverse and flexible employer.

    They are looking for an individual with several years of experience of clinical safety or pharmacovigilance within a CRO environment. The ideal candidate will currently be working under the same or closely aligned job title. Project management experience is preferred. Full proficiency within reviewing protocols and assessing all safety aspects of clinical trials. Weekly sponsor meetings to maintain clarity on on-going projects, ensuring set timelines are met.

    This position is remote for experienced candidates, however its is preferred if candidates are more junior or close to their offices then some attendance would be ideal. They have offices in Cincinnati, Dallas and Texas. Direct reports are dependent on seniority and WFH arrangements. You can expect a salary range between $90k-$125K + bonus with excellent benefits.

  • Clinical Operations

    $90000 - $140000 per annum, + bonus + excellent benefits
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    I am partnered exclusively with a World-class SME organisation at present to hire multiple Start-up roles – from Start-up Manager II to Associate Director level.

    The company is dedicated to developing their employees in the long term, meaning there is a good opportunity to expand scope of responsibility (including line management if desired). Candidates will be expected to have displayed a stable career background, they have very low turnover, we have had excellent feedback from recent placements, and they are a diverse and flexible employer.

    This role will be the primary point of contact for sponsors, also being involved in kick off/bid defence meetings, thus prior experience is required. The role will be very hand on with projects as opposed to providing just oversight, carrying the full workload of start-up of trials, handling on average 8 projects at any given time. Preferred therapy areas include oncology, cardiology, CNS and neurology but they are flexible, global experience also preferred. Experience levels can vary, looking for at least a couple years experience within an industry setting (ideally 4+ years in CRO). At level II & III there will be line management responsibilities, with AD/D level having additional managerial responsibilities.

    This position is remote contingent on a minimum of 4 years CRO experience, however it is preferred if candidates are more junior or close to their offices then some attendance would be ideal. They have offices in Cincinnati, Dallas and Texas. You can expect a salary of between $90-$140K + bonus + excellent benefits.