Fortrea

Global CRO providing Phase I-IV trials

CRA 2

Clinical Research OperationsConfirmed live in the last 24 hours

Full-timeMaidenhead, UKNo salary listed

Approximately 6–12 months of monitoring experience as a CRA I or CRA II.
A good understanding of International Council for Harmonisation Good Clinical Practice (ICH-GCP) and clinical trial processes.
Strong communication and relationship-building skills.
Comfort travelling regularly within the United Kingdom.

Monitor investigator sites across the North of England.
Build relationships with investigators and site teams.
Ensure patient safety, data quality, and regulatory compliance.
Conduct on-site and remote monitoring activities.
Travel to Oxford at least once per month, and attend an initial on-site onboarding and training period.

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:

The role requires travel to Oxford at least once per month, as well as an initial onboarding and training period on-site.

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!