About this role
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.
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.