Location

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

 

Be a part of a Queen’s Award winning company

EUDRAC is an expanding regulatory affairs and pharmacovigilance consultancy with offices in the UK, Germany and France.  If you are looking for a new challenge and want to work in a varied role, we are looking to recruit a number of Regulatory Affairs Consultants at a junior and senior level due to a number of exciting new projects.

 

About You

If you have experience in EU Regulatory (either pre- or post MAA), Regulatory Operations or CMC we have a role for you if you are the right fit for our team. Key criteria are an enthusiasm for regulatory affairs, the ability to demonstrate attention to detail, a willingness to learn, proven IT skills 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).

 

If you are looking for a new challenge in your career, please apply with you resume / CV and cover letter to: jobs@eudrac.com.

10 November 2021