Fortrea is currently seeking an In House CRA to join our multi-sponsor team in the UK. In this home-based, 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 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 CRO 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 .