CRA II - SCRA - Scotland

Fortrea; Maidenhead; On-site; GBP 42,000 - 54,000; Full time

Job summary

Fortrea is seeking an experienced CRA II or a SCRA1 to join our growing FSP team. This opportunity is based in Scotland, working on a variety of clinical studies while developing your expertise in a collaborative environment.

We value the ability to monitor study sites, ensure compliance and support patient safety, data integrity and study quality. Travel to investigator sites will be required as needed.

Qualifications

• Degree in Life Sciences or related healthcare/scientific discipline.
• 2+ years experience in clinical research (CRA or Site Management).
• Solid understanding of ICH-GCP, regulatory requirements and trial processes.

Responsibilities

• Conduct study site monitoring visits to ensure protocols, GCP, regulatory compliance and SOPs.
• Manage site activities including initiation, routine monitoring and closeout visits.
• Support patient safety, data integrity and overall study quality.
• Contribute to feasibility assessments, investigator engagement and vendor coordination.
• Build strong relationships with study sites and act as a trusted partner throughout the trial lifecycle.

Skills

Strong communication

Relationship-building

Organizational skills

Education

Life Sciences degree

Job 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 .