Head of Regulatory Affairs, Paris

My client, a pharmaceutical company based in Paris, are currently recruiting for a Head of Regulatory Affairs to join their growing team on a permanent basis.

The client conducts a major clinical development program in oncology as well as inflammatory and neurodegenerative diseases, including 13 phase 3 studies underway in 30 countries.

The ideal candidate will have 12-15 years of Regulatory Affairs exposure.

, Representing the company to health authorities
, Supervise the constitution and follow-up of regulatory files
, Participate in the drafting of registration files
, Participate in drafting regulatory responses to health authorities
, Managing the regulatory team
, Provide advice and assistance on regulatory aspects to the relevant departments

, Minimum 12-15 years of experience in regulatory affairs including 5 years in team and project management
, Significant experience in submission files and in drafting regulatory responses to local health authorities in launching studies in a country
, Significant experience(in pharmaceutical companies) in drafting regulatory responses and clinical study documents (protocol, investigative brochure, clinical report)
, Post-graduate science degree (Pharm.D, or Ph.D.)
, Essential running English
, Strong analytical capacity, strong working capacity, adaptability in a fast-growing environment

For further details about this role, or to discuss other vacancies within Regulatory Affairs, please contact Tim Barratt on +44(0)1727 817 626 or email a copy of your CV to tbarratt@keypeople.co.uk

  • Start: a.s.a.p
  • Rate: €100000 - €120000 per annum + bonus and benefi
  • Location: Paris, France
  • Type: Permanent
  • Industry: Pharmaceutical
  • Recruiter: Key People
  • Tel: +44 (0)1727 817 626
  • Fax: 01727 844 838
  • Email: to view click here
  • Posted: 2020-02-13 22:30:06 -

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