Merck Gruppe - MSD Sharp & Dohme in the United Kingdom is seeking a Clinical Trial Coordinator to oversee trial and site administration, ensuring timely handling of essential documents, CTMS updates, and close collaboration with COM, CRM and CRA to meet Site Ready dates.
The role includes supporting regulatory submissions to IRB/ERC and Health Authorities, managing CTRAs and payments with finance, and coordinating with country teams on labeling changes and translations as needed.
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Clinical Trial Coordinator — Site Start-Up & Documentation 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
