Senior Regulatory Affairs Consultant

Company
EUDRAC
Location
Oxfordshire, UK – hybrid working (3 days office, 2 remote)
Salary
Competitive
Posted
13 May 2021
Closes
12 Jun 2021
Discipline
Regulatory Affairs
Hours
Part Time
Contract Type
Permanent
Experience Level
Experienced (non-manager)

Senior Regulatory Affairs Consultant

Oxfordshire, UK – hybrid working (3 days office, 2 remote)

Be a part of a Queen’s Award winning company

EUDRAC is an expanding regulatory and pharmacovigilance consultancy company with offices in the UK, Germany and France. We are looking to recruit a Senior Regulatory Affairs Consultant with a good knowledge of European medicinal product regulatory affairs. The candidate must be able to demonstrate attention to detail, good IT skills, a willingness to learn and a ‘can do’ attitude.

Why EUDRAC?

* An opportunity to make a difference for patients – work focusses on novel products including ATMPs, often treating orphan diseases.

 

* Work in a company environment fostering a team spirit and an opportunity for you to make an impact.

 

* Diversified role and exposure to a variety of projects across a wide area of subjects - scientific advice, PIPs, orphan drug designations and centralised/UK registration procedures (pre- and post-authorisation).

 

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