CRA II (fixed-term)

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 .