Fortrea
CRA II (fixed-term)
United Kingdom · Work style not stated · Full time
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About the role
Description from the employer’s posting. Check the employer’s page for the current version.
- EmployerFortrea
- LocationUnited Kingdom
- Work styleWork style not stated
- Employment typeFull time
- Employer posted
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.
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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.
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At a glance
- Employment typeFull time
- Employer posted
- Added to ROLIVA
- Last checked
Skills in this posting
Skills ROLIVA found in the employer’s own description above. A mention is not a requirement.