Senior Site Study Coordinator (Non-Patient Facing)
SIRO Montpellier, France Posted 23 Aug 2026
About this role
Key Responsibilities: Provide advanced administrative support for clinical research studies. Oversee study operations and ensure compliance with protocols and regulatory requirements. Supervise and mentor junior study coordinators. Maintain high standards of study documentation and record-keeping. Collaborate with Principal Investigators (PIs), study teams, and sponsors to ensure study success. Prepare and manage regulatory submissions and communications. Monitor and report on study progress an…
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