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CRA II - SCRA - Scotland

fortrea
Companyfortrea
CategoryScience & Research
LocationMaidenhead
Remote
EmploymentNot stated
LevelMid
SalaryNot stated by the employer
Posted28 Jul 2026
Last verified9 Aug 2026
SourceEmployer ATS (workday)
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Description
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. We would love to hear from you! Learn more about our EEO & Accommodations request here .