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CRA II - SCRA - Scotland

Job in Maidenhead, Berkshire, SL6, England, UK
Listing for: Fortrea
Full Time position
Listed on 2026-07-30
Job specializations:
  • Science
    Clinical Research
Salary/Wage Range or Industry Benchmark: 35000 - 55000 GBP Yearly GBP 35000.00 55000.00 YEAR
Job Description & How to Apply Below

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 Scotland, 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.

EEO & Accommodations request.

At Fortrea, we're all about turning the “impossible” into "I'm possible." Together, we break barriers to deliver exceptional service to our patients, fueled by a shared commitment to teamwork and excellence. Regardless of your role, we're all family, working together to achieve extraordinary results. At Fortrea, your career isn't just a job – it's a journey of making the exceptional possible, every day.

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