Clinical Trial Coordinator
fortrea
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!
Learn more about our EEO & Accommodations request here.
You'll be redirected to fortrea's official application page on Workday.