We are seeking a CRA I or CRA II to support a routine post-market surveillance study within a dedicated FSP model.
Key responsibilities include:
- Monitoring investigator sites across the North of England.
- Building strong relationships with investigators and site teams.
- Ensuring patient safety, data quality, and regulatory compliance.
- Conducting on-site and remote monitoring activities.
About you
- CRA I or CRA II with approximately 6-12 months of monitoring experience.
- Good understanding of ICH-GCP and clinical trial processes.
- Strong communication and relationship-building skills.
- Comfortable travelling regularly within the UK.
- Motivated to continue developing your career in clinical research.
Learn more about our EEO & Accommodations request here.
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 (fixed-term) in Maidenhead employer: FTMAI Fortrea Development Ltd
Fortrea is an exceptional employer that fosters a collaborative work environment, where teamwork and dedication to patient service are at the forefront. With a hybrid working model in London, employees benefit from flexibility while gaining invaluable experience in complex oncological trials, alongside opportunities for professional growth in regulatory and TMF expertise. Join us to be part of a mission-driven team that values your contributions and supports your career development.
Contact Details:
FTMAI Fortrea Development Ltd Recruitment Team
