CRA II - SCRA - South-West

United Kingdom·Maidenheadmid

HealthcareClinical Researcher

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Quick Summary

Key Responsibilities

Conduct study site monitoring visits to ensure compliance with protocols, GCP, regulatory

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HealthcareClinical Researcher

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.

What We Offer

~1 min read

✓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.

Responsibilities

~1 min read

→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.

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.