Clinical Trial Coordinator

il y a 7 jours


Toulouse, Occitanie, France Pharmiweb Temps plein

As a Clinical Trial Assistant at Pharmiweb, you will play a vital role in the coordination and administration of study activities from start to close out. Key responsibilities include Trial Master File creation, data entry, and document management. Key Responsibilities:

  • Trial Master File (TMF) creation and management
  • Data entry and maintenance of local study data in study management systems
  • Collection, review, tracking, and provision of clinical documents to support regulatory submission
  • Managing study related supplies and facilitating their distribution to sites
  • Processing, reconciling, distributing, and tracking essential documents
  • Completing tracking documentation, including spreadsheets and study trackers
  • Preparing and reviewing site communication documents
  • Setting up and maintaining courier accounts and organizing shipments
Qualifications:
  • First stable experience as a CTA in the pharmaceutical industry or a CRO
  • Excellent organization and communication skills
  • Ability to work in a dynamic environment and prioritize tasks effectively
  • Strong IT skills and fluency in French and professional proficiency in English


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