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CRA II – UK (South / South East / Greater London based)
We’re supporting a growing, mid-sized, global Clinical Research Organisation (CRO) looking to hire a CRA II to support Phase I–IV and Real-World Evidence (RWE) studies.
This is a hands-on role with full ownership of sites, working across complex and rare disease trials within a collaborative, high-performing team.
What You’ll Be Doing
- Act as the primary contact for assigned sites
- Deliver all monitoring visits (SIV, IMV, COV) to a high standard
- Support start-up activities, site selection, and patient recruitment strategies
- Ensure compliance with ICH-GCP, SOPs, and regulatory requirements
- Manage TMF/ISF, Intellectual Property (IP) accountability, and site performance
- Identify risks and drive solutions at the site level
- Contribute to study delivery, data quality, and timeline adherence
- Mentor junior CRAs and potentially lead projects
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What We’re Looking For
Experience & Background
- 3+ years’ independent monitoring experience
- Strong background within a CRO (Clinical Research Organisation
- Experience in rare disease and/or transplant studies (preferable with pulmonary imaging)
- Solid knowledge of ICH-GCP and regulatory frameworks
- Confident in managing complex protocols and multiple sites simultaneously
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Logistics & Requirements
- Based in the UK (South / South East / Greater London region)
- Able to travel approximately 6–8 days per month
If you’re looking for greater ownership, exposure to complex studies, and a meaningful impact—this could be your next career move.
For further discussion, please apply and Harry Henson will get in touch.
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