Job Details

A company is looking for a Clinical Trials Data Coordinator.Key ResponsibilitiesEnsure data integrity for various research studies, including data abstraction and CRF completionCoordinate sponsor monitor visits and maintain audit-ready dataOversee electronic research records and patient information in the CTMSRequired Qualifications and EducationBachelor's Degree, or relevant experience may substitute for degreeAt least two years of experience related to the conduct of oncology clinical trialsWorking knowledge of clinical trials, Federal, State, and Local Regulations, and IRB requirements