At a Glance
- Tasks: Conduct site monitoring visits and ensure compliance with clinical trial protocols.
- Company: Fortrea, a global leader in advancing healthcare and improving patient outcomes.
- Benefits: Flexible work environment, ongoing career development, and supportive team culture.
- Other info: Join a collaborative team that values mentorship and professional growth.
- Why this job: Make a real impact on patients' lives while growing your clinical research career.
- Qualifications: Degree in Life Sciences and 2 years of clinical research experience required.
The predicted salary is between 37000 - 45000 £ per year.
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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CRA II - SCRA - Scotland in Maidenhead employer: Fortrea
Fortrea is an exceptional employer that fosters a dynamic and collaborative work culture in Maidenhead, England. With a strong emphasis on employee growth and development, we offer comprehensive training programs and opportunities for advancement within the pharmaceutical sector. Our commitment to innovation and client success ensures that you will play a pivotal role in shaping the future of healthcare while enjoying a supportive environment that values your contributions.
