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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Remote CRA: Site Monitoring & Leadership, UK Trials employer: Merck Gruppe - MSD Sharp & Dohme
As a global healthcare leader, we offer an exceptional work environment that prioritises integrity, teamwork, and innovation. Our Medical Science Liaison role in the North of England, Scotland & Northern Ireland provides unique opportunities for professional growth through collaboration with healthcare professionals and involvement in impactful projects. We are committed to fostering an inclusive culture where diverse ideas thrive, ensuring that our employees feel valued and empowered to contribute to a healthier future.
Contact Details:
Merck Gruppe - MSD Sharp & Dohme Recruitment Team
