Clinical Trial Assistant

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Pharmaceutical Research Associates, Inc
Paris
EUR 35 000 - 55 000
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Il y a 7 jours
Description du poste

Overview

As a Clinical Trial Assistant, you will be dedicated to one of our global pharmaceutical clients with whom ICON shares a culture of innovation, flexibility, and a common vision of bringing life-improving drugs to market. Leading by example, you can set the standard of excellence and enjoy a challenging career in our exclusive programs.

We are currently looking for a Clinical Trial Assistant to join one of our sponsor-dedicated teams in Puteaux (3 days office based).

Responsibilities

The Clinical Trial Assistant assists in the coordination and administration of the study activities from the start-up to execution and close-out, and within the Local Study Team to ensure quality and consistency of interventional study deliverables to time, cost, and quality objectives. As a Clinical Trial Assistant, you will have the opportunity to experience the full lifecycle of a project and genuinely contribute to drug development and improving patients’ lives.

Key responsibilities include:

  • Trial Master File (TMF) creation and management
  • Coordinate entry and maintain local data into study management systems including setting up new studies
  • Ensure collection, review, tracking, and provision of appropriate clinical documents to support regulatory submission
  • Track and maintain adequate study-related supplies in the office and facilitate their distribution to sites, including preparing and distributing Study File Binders and Site Initiation presentations/materials
  • Process, reconcile, distribute, and track essential documents and submit them to local archive in compliance with SOPs
  • Complete tracking documentation as applicable including but not limited to spreadsheets, study, and contract tracker
  • Prepare and review site communication documents
  • Set up/maintain courier accounts and organize shipments

Qualifications

You will need:

  • A first stable experience as a CTA, within the pharmaceutical industry or a CRO
  • Excellent organization skills
  • Ability to work well in a dynamic environment and prioritize and respond to changing needs of the business
  • Strong IT skills
  • Strong communication skills with the ability to multitask and work effectively under pressure
  • Fluency in French and professional proficiency in English
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