Remote CRA: Site Monitoring & Leadership Trials
Liverpool, Merseyside, L1, England, UK
Listed on 2026-10-25
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Research/Development
Clinical Research
Merck & Co., Inc. in the UK is seeking a Clinical Research Associate to lead site monitoring and ensure ICH/GCP compliance across assigned trials.
You will build relationships with investigative sites and manage documentation in CTMS/eTMF, supporting audits and regulatory findings. The role requires travel of 65–75% (about 2–3 days per week) domestically and internationally, mentoring junior CRAs, and collaborating with cross-functional teams to drive site readiness and study execution in a
We would love to welcome a new Remote CRA:
Site Monitoring & Leadership, UK Trials to our organisation in United Kingdom.
If your experience matches this role, we encourage you to apply.
All applications are reviewed carefully by our team.
The position is based in United Kingdom.
This opportunity is part of our work in Bio & Pharmacology & Health.
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