Merck is seeking a Clinical Trials Coordinator to support trial and site administration, document management, budgeting, and regulatory submissions. The role collaborates with COM, CRM, CRA, and finance to ensure CTRAs, payments, and site readiness.
The successful candidate will manage eTMF processes, update study tools, coordinate translations, and support IRB/ER submission packages, while ensuring compliance with GxP guidelines and local regulations.
#J-18808-LjbffrRemote Clinical Trial Coordinator: Site & Docs Mastery in dover at Unknown Company
This position is listed as full time and onsite.