Clinical Trial Administrator/Project Coordinator
Fortrea is currently seeking a Clinical Trial Administrator/Project Coordinator to join our client-dedicated team in the UK. In this hybrid role, you’ll play a key part in supporting global clinical trials across all phases, working closely with Clinical Trial Leaders and cross-functional teams to ensure smooth trial delivery.
Location: Remote, with occasional travel to Bracknell (1–2x/month)
Type: Full-time, permanent
What You’ll Do:
1. Coordinate trial planning, setup, conduct, and closeout activities in line with ICH-GCP standards.
2. Manage internal and external systems, track trial progress, and maintain documentation (including TMF).
3. Collaborate with internal teams, CROs, vendors, and investigators to support trial execution.
4. Support trial submissions and the preparation of Clinical Trial Reports.
What You’ll Need:
1. University degree or equivalent experience in clinical research.
2. Experience in trial administration within an international environment.
3. Solid knowledge of ICH-GCP and major regulatory frameworks (FDA, EMA, PMDA).
4. Excellent communication skills and proficiency with MS Office tools.
Why Apply:
1. Home-based flexibility with minimal travel
2. Stable, long-term opportunity with a leading client
3. Attractive salary and benefits package
Interested in making a meaningful impact in clinical research? We’d love to hear from you!
Learn more about our EEO & Accommodations request here.
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