Social network you want to login/join with:
Clinical Trial Administrator/Project Coordinator, Maidenhead
col-narrow-left
Client:
Location:
Job Category:
Other
-
EU work permit required:
Yes
col-narrow-right
Job Reference:
f042ad05a0db
Job Views:
6
Posted:
05.05.2025
Expiry Date:
19.06.2025
col-wide
Job Description:
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:
* Coordinate trial planning, setup, conduct and closeout activities in line with ICH-GCP standards.
* Manage internal and external systems, track trial progress and maintain documentation (including TMF).
* Collaborate with internal teams, CROs, vendors and investigators to support trial execution.
* Support trial submissions and the preparation of Clinical Trial Reports.
What You’ll Need:
* University degree or equivalent experience in clinical research.
* Experience in trial administration within an international environment.
* Solid knowledge of ICH-GCP and major regulatory frameworks (FDA, EMA, PMDA).
* Excellent communication skills and proficiency with MS Office tools.
Why Apply:
* Home-based flexibility with minimal travel
* Stable, long-term opportunity with a leading client
* 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. #J-18808-Ljbffr