Merck seeks a Clinical Trial Documentation & Site Administration professional to manage trial documents, CTMS updates, and regulatory submissions. The role supports site readiness, budgeting, and contract processes while coordinating with investigators and internal teams.
Strong document control and communication skills are essential. Remote-friendly position with a focus on global clinical trials; requires Bachelor’s degree or equivalent training and English proficiency.
#J-18808-LjbffrRemote Clinical Trial Coordinator - Docs & Budgets in augusta at Unknown Company
This position is listed as contract and able to be worked remotely.