Job Details

A company is looking for a Senior Clinical Trial Coordinator.Key ResponsibilitiesManage the Trial Master File (TMF) and Investigator Site File (ISF) for clinical studiesTrack and review study-specific documents and manage device accountabilityOversee study budgets, payments, and maintain audit readiness of study documentationRequired QualificationsBA/BS or equivalent experience in scientific or healthcare disciplinesMinimum of two years of experience in clinical research, preferably with medical device or pharmaceutical trialsProficiency in MS Windows-based applicationsWorking knowledge of ICH Good Clinical Practice guidelinesValid driver's license and ability to travel domestically up to 10%