Job Details

A company is looking for a Clinical Trials Data Coordinator.Key ResponsibilitiesEnsure data integrity for various research studies through data abstraction and CRF completionCoordinate sponsor monitor visits and maintain audit-ready dataOversee electronic research records and patient information in the CTMSRequired QualificationsBachelor's Degree, with relevant experience as a substituteAt least two years of experience related to the conduct of oncology clinical trialsWorking knowledge of clinical trials, Federal, State, and Local Regulations, and IRB requirementsIn-depth knowledge of Good Clinical Practices (GCP), FDA regulations, NIH guidelines, and HIPAA regulations