Sr Clinical Research Associate Contractor (France)

Allucent

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Role summary

Allucent seeks an experienced Clinical Research Associate contractor to lead monitoring activities across clinical trials in France on a hybrid basis. The role involves independent site management, regulatory compliance oversight, and collaboration with investigators to ensure study integrity and protocol adherence.

Where this listing comes from

This listing was compiled by RoleLantern from the employer's publicly available posting on Workable, captured and rephrased by RoleLantern using automated (AI) tools on 2026-10-03 (originally posted 2026-10-03). It was not submitted or confirmed by the employer through RoleLantern. Details may be inaccurate, incomplete, outdated, or no longer available; please confirm with the employer's official posting before applying.

What they're looking for

Minimum 5 years' experience leading monitoring activities in complex trials
Background in oncology or rare disease preferred
Strong knowledge of ICH-GCP and regulatory guidelines
Fluent in English and Hebrew
Ability to work independently and manage multiple priorities
Willingness to travel as required

What you'll be doing

Independently manage all monitoring aspects including site initiation, routine visits, and close-out activities
Ensure compliance with protocols, GCP guidelines, ICH standards, and regulatory requirements
Develop and maintain strong relationships with investigator sites as primary contact
Identify, troubleshoot, and resolve site issues to maintain trial integrity
Support regulatory affairs, site activation, and study startup processes

Privacy & handoff

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