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.
The role requires travel to Oxford at least once per month, as well as an initial onboarding and training period on-site.
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.
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CRA II (fixed-term) in Maidenhead employer: Fortrea
Fortrea is an exceptional employer that offers a rewarding and meaningful work environment, particularly for Senior Technical Designers. With a strong support network, flexible working solutions, and a commitment to employee growth, you will thrive in a collaborative workspace that values diversity and inclusion. Enjoy competitive compensation packages and the opportunity to make a significant global impact while maintaining a genuine work-life balance.
