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Clinical Project Manager

France   •  EUR50000 - EUR70000 per annum  •  Permanent, Full time


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


* 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

You MUST be eligible to work in France. Learn more

  • Agency: Key People
  • Reference: DT24097
  • Posted: 15th March 2019
  • Expires: 22nd March 2019

Key People

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