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Current vacancies listed in detail.

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Job List - United Kingdom

Senior CRA/PM

Job Type: Permanent
Location: United Kingdom, United Kingdom_Home based,
Salary: Competitive

Working for this dynamic and innovative CRO, you will be joining an established and professional team working in a variety of therapy areas in all Phases of Clinical Research. This position will offer applicants the ability to grow and develop their professional skills and career in a supportive environment. The successful candidate is required to have oncology experience.

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Senior CRA

Job Type: Permanent
Location: United Kingdom, Yorkshire,
Salary: Competitive

A global medical device company have a vacancy for a Senior CRA for a twelve month contract to assist with ongoing clinical studies.

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Associate Director of Regulatory Affairs

Job Type: Permanent
Location: United Kingdom, Manchester,
Salary: Competitive

An innovative market and technology leader are seeking to recruit an Associate Director of Regulatory Affairs. Key criteria for the succesful candidate is to have extensive experience in both the medical device industry and regulatory experience. Working as part of a global regulatory team spread across 35 locations worldwide.

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Senior Regulatory Associate

Job Type: Permanent
Location: United Kingdom, Yorkshire,
Salary: Competitive

A leading UK pharmaceutical company are currently undergoing a UK expansion plan which included the acquisition of a medical device division. The global regulatory affairs department are currently looking to recruit regulatory professionals with specific experience of the medical device products. This is an exciting opportunity to join a global team within a global blue chip client.

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Associate Director - Regulatory Affairs

Job Type: Permanent
Location: Belgium, United Kingdom,
Salary: Competive

Working with a global leader in the biopharmaceutical industry who are currently expanding their capabilities in the area of medical devices. You will be working in a global regulatory team spread across 5 locations in Europe and US. The key criteria is for the succssful candidate to have experience of both CMC and medical device regulatory experience as relevant to combination products. This is an exciting role for a progressive company who are looking to upskill their department. You will also be responsible for managing a team.

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