Senior CRA II - Sponsor dedicated

Fortrea; Paris; Remote; EUR 60,000 - 85,000; Full time

Benefits offered by this job

Career growth environment

Dedicated Line Manager

Work with leading sponsor

Competitive salary and FortreaBenefits

Job summary

Fortrea’s Paris office is seeking a Senior Clinical Research Associate II (SCRA II) to monitor clinical trials, oversee site operations and ensure GCP compliance across France. The role involves site visits, data verification, and collaborating with investigative sites to maintain study integrity.

Responsibilities include SDV, investigator training, and thorough study documentation. The position offers office-based or remote work options and a pathway for career growth within a leading sponsor,

Qualifications

• Life Sciences degree or allied health certification.
• Understanding of ICH GCP Guidelines and local regulations.
• Knowledge of monitoring procedures and clinical trial process.
• Fluency in English (written and spoken).

Responsibilities

• Monitor clinical trials with site visits to ensure protocol and GCP compliance.
• Site management as primary contact for investigational sites and smooth study operations.
• Review and verify accuracy of clinical data from study sites (SDV).
• Provide investigator training and support on study protocols and regulatory requirements.
• Prepare monitoring reports and maintain study documentation.

Skills

GCP knowledge

Clinical monitoring

Site management

English fluency

Education

Life Sciences degree

Job description

Fortrea is recruiting!

Our FSP department in Paris is looking for a 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 degree or certification in a related allied health profession from an appropriately accredited institution (e.g., nursing licensure).
• Thorough understanding of ICH GCP Guidelines and understanding of local regulatory requirements.
• Thorough knowledge of monitoring procedures and 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!

Learn more about our EEO & Accommodations request here.