Kettering Health is a not-for-profit system of 13 medical centers and more than 120 outpatient facilities serving southwest Ohio. We are committed to transforming the health care experience with high-quality care for every stage of life. Our service-oriented mission is in action every day, whether it’s by providing care in our facilities, training the next generation of health care professionals, or serving others through international outreach.
Kettering Health Main Campus
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.
This individual must be able to work independently under limited supervision, while maintaining excellent communication between the principal investigator(s) and all staff involved in any aspect of approved research projects.