Site Research Assistant (Part‑time, Independent Contractor)

About the role

IQVIA is seeking a Site Research Assistant to join a clinical trial team in Nantes on a part‑time basis. The position starts in June 2026, runs for approximately six months, and is offered as an independent‑contractor role. You will work on‑site, supporting the Principal Investigator in delivering a safe and compliant study.

Key responsibilities

• Maintain up‑to‑date study documentation, including protocols, case report forms and electronic data capture (EDC) systems.
• Assist with patient screening, enrolment and informed‑consent procedures.
• Plan and coordinate study activities in line with protocol requirements.
• Perform data entry, conduct data quality checks and resolve queries.
• Manage shipment of biological samples and liaise with study monitors.
• Provide general administrative support to ensure smooth study operations.

Required profile

• Bachelor’s degree in Life Sciences or equivalent, or relevant clinical/medical experience.
• 1–2 years of experience as a Clinical Research Assistant or Coordinator at a site level.
• Good understanding of clinical trial processes, protocols and study documentation.
• Fluent French language skills.

Required skills

• Microsoft Excel
• Microsoft Word
• Microsoft Outlook
• Electronic Data Capture (EDC) systems

What we offer

• Hands‑on experience across the full clinical trial lifecycle.
• Flexible 16‑hour‑per‑week schedule, ideal for balancing other commitments.
• Opportunity to work with a global leader in clinical research.