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.