CRA II SCRA South-West

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 youll 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
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• 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 Were 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
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• Strong communication relationship-building and organizational skills.
• A proactive approach to problem-solving and managing priorities.
• A valid drivers licence and willingness to travel to investigator sites as required.

At Fortrea youll 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.