Fortrea is currently seeking a proactive In-house Clinical Research Associate to join our expanding team in the UK. This is a home-based role.
What You’ll Do:
Communicate with project teams and track study activities
Maintain essential documentation and ensure regulatory compliance
Support site and study material preparation
Assist with meeting coordination, minute-taking, and documentation
Manage Trial Master File (TMF) documentation and quality control
Liaise with vendors and coordinate study supply shipments
Provide general administrative and systems support
Requirements:
* Minimum of 12 months’ experience in Clinical Research Administration (e.g. Study Coordinator, CRA internship etc)
* Experience supporting clinical trials in the UK is preferred
* Strong ability to work independently and manage time effectively
* Basic understanding of biology and clinical trial processes
* Excellent organizational and communication skills
Why Join Us?
This role provides an excellent opportunity to support CRAs in the delivery of complex, high-quality clinical trials in the UK. It’s a chance to develop your skills in a supportive team and contribute to impactful studies.
Learn more about our EEO & Accommodations request here. #J-18808-Ljbffr