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Requisition ID 25196/*generated inline style */ Country France/*generated inline style */ Location type Hybrid/*generated inline style */ State / Province Paris/*generated inline style */ City Pari... Voir plus

Our FSP department in Paris is looking fora Senior Clinical Research Associate II (SCRA II).

Key Responsibilities:

Monitor Clinical Trials -conduct site visits to ensure compliance with protocols regulatory requirements and Good Clinical Practice (GCP) - National on sites visits in France (40%).

Site Management- Serve as the primary point of contact for investigational sites ensuring smooth study operations.

Source Document Verification (SDV)- Review and verify accuracy of clinical data collected from study sites.

Investigator Training and Support- Provide ongoing training to site staff on study protocols and regulatory requirements

Reporting and Documentation- Prepare monitoring reports maintain study records and contribute to overall trial documentation.

Qualifications:

Life Sciences University degreeorcertification in a related allied health professionfrom an appropriately accredited institution (e.g. nursing licensure).

Thorough understanding ofICH GCP Guidelinesand understanding oflocal regulatory requirements.

Thoroughknowledge of monitoring proceduresand basic understanding of the clinical trial process.

Fluency in English written and verbal.

What We Offer:

Office based or remote position

Career growth environment in a supportive environment

Dedicated Line Manager

Works directly with a leading sponsor on innovative studies

Attractive salary and Fortrea benefits

If you are passionate about clinical research thrive in a collaborative environment and seek exciting career growth we want to hear from you!

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