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CRA II SCRA Scotland

Fortrea


Job Location:

Maidenhead - UK

Monthly Salary: Not provided by the employer
Posted: 11 August 2026 (13 days ago)
Application Deadline: 8 November 2026
Vacancies: 1 Vacancy

Job Summary

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 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.
  • 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.
  • 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.


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