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Fortrea

CRA II (fixed-term)

Maidenhead

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hirly's read of this role

Seniority
Mid level
Country
GB
Work mode
On-site / unstated
First seen by hirly
27 Sept 2026

Derived automatically from the posting. Upload your resume above to see how the role scores against it.

the posting

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 .

Original posting on Fortrea's site ↗

Listed on hirly, a job board. hirly is not the employer: Fortrea is hiring for this role.

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