Fortrea
Senior CRA II - Sponsor dedicated
France · Work style not stated · Full time
Apply on the employer’s site ↗See how well you match this job
You apply directly with the employer. ROLIVA does not submit applications from this page and is not the employer.
About the role
Description from the employer’s posting. Check the employer’s page for the current version.
- EmployerFortrea
- LocationFrance
- Work styleWork style not stated
- Employment typeFull time
- Employer posted
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).
Show full description
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.
Check your resume against this job Free, no sign-up. Nothing you paste is stored.
Staying safe while you apply
- Never pay to apply, interview or accept an offer. ROLIVA never asks you for payment to apply to a job.
- Apply only through the official “Apply on the employer’s site” button, on the employer’s own site, and check that a recruiter’s email uses that employer’s own domain rather than a free email address.
- Be cautious of an offer made with no real interview, or pressure to decide quickly or share financial details early.
Does something look wrong with this listing? Use “Report broken link” in the role details, or read ROLIVA’s full job-safety guidance ↗.
Preparing for this role with ROLIVA
- Check the fit.
Compare the requirements with the experience you have confirmed, including gaps.
- Prepare honestly.
Build interview stories and application drafts from your own evidence.
- Keep track.
Save the role and record your own application status and follow-ups.
At a glance
- Employment typeFull time
- SenioritySenior
- Employer posted
- Added to ROLIVA
- Last checked
Skills in this posting
Skills ROLIVA found in the employer’s own description above. A mention is not a requirement.