About this role
Are you looking to take the next step in your clinical research career? Fortrea is seeking an experienced CRA II or a SCRA1 to join our growing FSP team.
This is a fantastic opportunity for candidates based in the South-West region (Bristol/Bath/Swindon/Gloucester/Cheltenham/Cardiff/Exeter area), where you'll work on a variety of clinical studies while developing your expertise in a supportive, collaborative environment.
Why Join Fortrea?
- Be part of a global, innovative organization helping to advance healthcare and improve patient outcomes.
- Gain exposure to a diverse portfolio of clinical trials across multiple therapeutic areas.
- Enjoy ongoing career development and opportunities for progression within our CRA community.
- Join a supportive team culture that values collaboration, mentorship, and professional growth.
- Benefit from the flexibility and stability of working within a strong FSP partnership.
Key Responsibilities:
- Conduct study site monitoring visits to ensure compliance with protocols, GCP, regulatory requirements, and company SOPs.
- Manage all aspects of site activities, including site initiation, routine monitoring, and closeout visits.
- Support patient safety, data integrity, and overall study quality.
- Contribute to feasibility assessments, investigator engagement, and vendor coordination activities.
- Build strong relationships with study sites and act as a trusted partner throughout the clinical trial lifecycle.
- Track and report Serious Adverse Events (SAEs) as required.
- Support less experienced team members and contribute to continuous quality improvement initiatives.
What We're Looking For:
- Degree in Life Sciences or a related healthcare/scientific discipline.
- Minimum 2 years of experience in clinical research, such as a CRA or Site Management role.
- Good understanding of ICH-GCP, regulatory requirements, and clinical trial processes.
- Strong communication, relationship-building, and organizational skills.
- A proactive approach to problem-solving and managing priorities.
- A valid driver's licence and willingness to travel to investigator sites as required.
At Fortrea, you'll have the opportunity to make a meaningful impact on patients' lives while continuing to grow your clinical research career alongside experienced and passionate professionals. We would love to hear from you!
Learn more about our EEO & Accommodations request here.
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