Clinical Research Coord I - Innovate and Research
Job
Kettering Health
Thurman, OH (In Person)
Full-Time
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Job Description
Job Details Kettering Health Main Campus| Kettering | Full Time| Days Responsibilities & Requirements The Clinical Research Coordinator I (CRC I) is a professional with clinical research expertise preferred. Under the supervision of the Manager, Innovation, Research & Grants at KHN, the CRC I will collaborate with physicians and other healthcare providers, scientists, administration, the Institutional Review Board, Sponsors, and the Food and Drug Administration (FDA). The CRC I is responsible for assisting the Investigator in accomplishing successful research trials. The CRC I is expected to adhere to Good Clinical Practice (GCP) guidelines as set forth by the Federal regulations. The CRC I will screen, enroll, and follow study subjects, ensuring protocol compliance and close monitoring of the subjects participating in the research study. The CRC I is responsible for all data reporting via source documents including adverse event reporting. Maintenance of complete regulatory files will be coordinated with the Regulatory Documentation Specialist (RDS). Depending on the requirements of a specific protocol, other duties may be assigned based upon the CRC's qualification, training, experience and licensure, when applicable. The CRC I will adhere to policies of the Innovation, Research & Grants related to compliance of Federal regulatory issues, education, training, and GCP.