Location: UK - Midlands
Contract: 12-month fixed-term (with potential extension based on business needs)
Model: Client‑dedicated role (FSP)
What you’ll do:
- Conduct and oversee site monitoring visits in line with protocols and regulatory requirements
- Manage site activities from initiation through to closeout
- Ensure patient safety, data integrity, and GCP compliance
- Support feasibility, site selection, and vendor coordination
- Contribute to team development and quality improvement efforts
Qualifications:
- Degree in life sciences or a related field
- Minimum 2 years’ experience in clinical research (e.g., CRA, Site Management)
- Knowledge of regulatory guidelines and clinical trial processes
- Strong communication and organizational skills
- Willingness to travel and a valid driver’s license
Learn more about our EEO & Accommodations request here.
CRA II, client-dedicated (fixed-term) in Maidenhead employer: FTMAI Fortrea Development Ltd
Fortrea is an exceptional employer that fosters a culture of innovation and accountability, making it an ideal place for professionals seeking to make a meaningful impact in clinical technology. With a strong focus on employee growth opportunities, Fortrea offers a collaborative environment where leaders can drive product strategy and operational excellence while working with cutting-edge technologies. Located in a dynamic industry, employees benefit from competitive compensation, comprehensive benefits, and the chance to be at the forefront of transforming clinical trials and patient experiences.
Contact Details:
FTMAI Fortrea Development Ltd Recruitment Team
