Clinical Trial Coordinator

il y a 4 semaines

Lille, Hauts-de-France Pharmiweb Temps plein

About the Role:

We are seeking a highly organized and detail-oriented Clinical Trial Assistant to join our team in Issy-Les-Moulineaux. As a Clinical Trial Assistant, you will be responsible for coordinating and administering study activities from start-up to execution and close-out.

Key Responsibilities:

  • Creation and management of Trial Master Files (TMFs)
  • Coordination of entry and maintenance of local data into study management systems
  • Collection, review, tracking, and provision of clinical documents to support regulatory submission
  • Tracking and maintenance of study-related supplies, including distribution to sites
  • Processing, reconciliation, distribution, and tracking of essential documents
  • Preparation and review of site communication documents
  • Setup and maintenance of courier accounts and organization of shipments

Requirements:

  • First stable experience as a Clinical Trial Assistant in the pharmaceutical industry or a CRO
  • Excellent organization skills
  • Ability to work well in a dynamic environment and prioritize tasks
  • Strong IT skills
  • Strong communication and multitasking skills
  • Fluency in French and professional proficiency in English

About ICON:

At ICON, we value diversity, inclusion, and belonging. We strive to create an inclusive environment that fosters innovation and excellence. We offer a range of benefits, including competitive salary, annual leave entitlements, health insurance, retirement planning, and more.

How to Apply:

Interested candidates should submit their application through our careers site. We welcome applications from motivated and dedicated individuals who share our values and are passionate about making a difference in the pharmaceutical industry.

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