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Job Reference: SC/RA

Regulatory Affairs Manager

  • Paris, Île-de-France, France
  • Contract / Full Time
  • Life Sciences Team
  • £260 - £530

My client is looking for an RA Consultant on a full time basis to help them through their clinical phases with multiple products.Below is a list of criteria you should meet to be eligible for the vacancy:

  • Have at least 5 years experience in Regulatory Affairs
  • Have experience in managing regulatory aspects of multinational European Clinical trials including initial submissions, questions – including proposing response, aggregate reporting
  • Ideally some experience in European centralized procedures eg Scientific Advise, PrIME, Peds, Orphan
  • Ideally have experience in drug development particularly clinical aspects
  • Speak fluent English
  • Ability to handle internal stakeholders and external vendors

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