Clinical Project Manager

Missions:

Design, implementation and coordination of clinical studies with the support of Clinical Operations, Pharmacovigilance, Biometrics and Medical Writing departments:
, Plan the clinical development program
, Draft protocols, amendments and study reports
, Prepare regulatory files
, Manage relationships with investigators and opinion leaders
, Implementation and follow-up of actions to meet recruitment deadlines and good clinical practice


Profile:

, Additional training in methodology (CESAM, IUD, ...)
, Successful experience as a Clinical Project Manager in a pharmaceutical or CRO laboratory
, 6 to 8 years of clinical development experience (Phase II and III)
, Experience in oncology or in autoimmune inflammatory diseases
, Experience of international development required
, Control of the regulatory environment for clinical trials
, Experience in the drafting of FDA (IND, NDA) and EMA
, Fluent English


  • Start: ASAP
  • Rate: €50000 - €70000 per annum
  • Location: Paris, France
  • Type: Permanent
  • Industry: Pharmaceutical
  • Recruiter: Key People
  • Tel: 01727 817 638
  • Fax: 01727 844 838
  • Email: to view click here
  • Posted: 2019-03-29 16:59:10 -

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