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!