Description
The Clinical Study Administrator supports the coordination of clinical trials from start-up through execution and close-out in Country Operations Management. Responsibilities include trial deliverable quality and timeliness, electronic Trial Master File setup and maintenance, regulatory document tracking, CTMS milestone management, site-file preparation, clinical trial supply coordination, project communications, global process standardization, regulatory submissions, and local study meetings. The role requires at least three years of experience, a bachelor's degree, life-science or drug-development knowledge, and strong organizational and communication skills. The annual base pay is $82,798 to $124,196, with health, dental, and vision coverage.
