Merck is seeking an experienced Clinical Trial Coordinator/CTC to oversee trial and site administration, document management, and regulatory submissions. You will collaborate with local and country teams on CTRAs, budgets, and payments, while ensuring timely study tool distribution and eTMF quality control.
The role requires strong MS Excel/Office skills, knowledge of ICH-GCP, and the ability to work in a matrix multicultural environment. Remote work arrangements are available.
#J-18808-LjbffrRemote Clinical Trial Coordinator: Site & Docs Lead in montpelier at Unknown Company
This position is listed as full time and able to be worked remotely.