Clinical Trial Coordinator
il y a 4 semaines
At Pharmiweb, we're seeking a highly organized and detail-oriented Clinical Trial Assistant to join our team. As a Clinical Trial Assistant, you will play a crucial role in the coordination and administration of study activities from start-up to execution and close-out.
Key responsibilities include:
- Creating and managing the Trial Master File (TMF)
- Coordinating entry and maintaining local data into study management systems
- Ensuring collection, review, and provision of clinical documents to support regulatory submission
- Tracking and maintaining study-related supplies and facilitating their distribution to sites
- Processing, reconciling, and distributing essential documents and submitting them to local archive in compliance with SOPs
- Completing tracking documentation as applicable
- Preparing and reviewing site communication documents
- Setting up and maintaining courier accounts and organizing shipments
Requirements:
- A first stable experience as a Clinical Trial Assistant, preferably within the pharmaceutical industry or a CRO
- Excellent organization skills and ability to work well in a dynamic environment
- Strong IT skills and fluency in French and professional proficiency in English
What We Offer:
At Pharmiweb, we value our employees and offer a range of benefits to support their well-being and work-life balance. These include various annual leave entitlements, health insurance options, competitive retirement planning, and a global Employee Assistance Programme. We're committed to providing an inclusive and accessible environment for all candidates and welcome applications from diverse backgrounds.
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