Remote CRA: Site Monitoring & Leadership, UK Trials

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

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