Position Summary

The Clinical Research Coordinator II (CRC-II) RN is responsible for the coordination of all day-to-day clinical research activities with minimal supervision. The CRC-II RN is assigned more complex studies, including but not limited to Phase II and Phase III therapeutic clinical trials for various types or stages of cancer. The CRC-II RN is responsible for coordinating multiple clinical trials simultaneously, ensuring full compliance with each research protocol, adhering to applicable federal regulations, Good Clinical Practice (GCP), SJ/C Policies & Procedures, and Institutional Review Board (IRB) requirements. The CRC-II RN works with clinical investigators to recruit diverse research participants representative of the site’s catchment area. Key tasks of the CRC-II RN include but are not limited to the following: obtaining informed consent, confirming participant eligibility, coordinating participant schedules to comply with research protocol requi...