CRA II - SCRA - Scotland
fortrea
| Company | fortrea |
| Category | Science & Research |
| Location | Maidenhead |
| Remote | — |
| Employment | Not stated |
| Level | Mid |
| Salary | Not stated by the employer |
| Posted | 28 Jul 2026 |
| Last verified | 9 Aug 2026 |
| Source | Employer ATS (workday) |
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 .