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 .