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Clinical Studies Project Manager

  1. France
Paris
  1. Contract
Competitive
  1. Drug Safety / Pharmacovigilance
02-06-2023
30603

This vacancy has now expired

Clinical Studies Project Manager – Pharmacovigilance – 6 Month Contract – Paris

This is a unique opportunity for a Clinical Studies Project Manager to join our client – an esteemed partner for regulatory and compliance in healthcare. This is a contract opportunity of at least 6 months within the stunning city of Paris but excellent potential to extend beyond this point. With a globally established presence spanning over 140 countries and partner to some of the top pharmaceutical companies, this is a fantastic company to join to progress your career.

Clinical Studies Project Manager Responsibilities:
  • Realisation of the feasibility of a new study
  • Define and review of the budget envelope and human resources to be allocated for the projects
  • Plan and coordinate each study
  • Manage various contracts (hospitals, investigators, subcontractors, confidentiality agreement, letter of intent, etc.)
  • Identify and follow-up with partners (CROs and others): permanent communication, organisation and conduct of teleconferences and follow-up of projects
  • Participate in the selection of investigation centres in coordination with the KOLs
  • Submit regulatory studies
  • Collect, prepare and draft various documents and guides necessary for the smooth running of the projects (monitoring guide, communication plan, etc.)
About you:
  • Knowledge of clinical trial regulations (ISO14155, ICH E6, MDR…
  • At least 3 years of experience as a clinical project manager in a pharmaceutical or medical device company or in a CRO.
  • French speaking (English language a plus)
Are you a good fit for this Clinical Studies Project Manager position? Get in touch with us today.

The candidate must have the rights to work in the location stated in the job advert.

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