Senior Clinical Research Associate I - Sponsor dedicated

Fortrea is recruiting!

Fortrea in Paris is looking for a Senior Clinical Research Associate I (SCRA I) to be Sponsor-Dedicated.

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Key Responsibilities

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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%).

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

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

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

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

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​​Qualifications

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Life Sciences University degree or certification in a related allied health profession from an appropriately accredited institution (e.g., nursing licensure).

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Thorough understanding of ICH GCP Guidelines and understanding of local regulatory requirements.

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Thorough knowledge of monitoring procedures and basic understanding of the clinical trial process.

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Fluency in English, written and verbal.

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What We Offer

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Office based or remote position

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Career growth environment in a supportive environment

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Dedicated Line Manager

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Attractive salary and Fortrea benefits

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

Learn more about our EEO & Accommodations request here .