DescriptionWe 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 youCRA 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.
If you're looking to build your monitoring experience within a supportive team and a well-established study environment, we'd love to hear from you!
Learn more about our EEO & Accommodations request here. 
