Clinical Research Coordinator I, Cancer Center

This clinical research coordinator position is responsible for coordinating a clinical trial patient through all protocol-required procedures. This includes, but is not limited to, consenting, screening, collecting and entering data, and performing follow-up for all patients on assigned clinical trials. The coordinator serves as the liaison between regulatory staff, research RNs, clinic staff, clinical faculty, and the research sponsor to carry out protocol-required events, including data entry, as determined by the protocol calendars. The coordinator supports clinical research protocols from the site evaluation visit, site initiation visit, and start-up through study closure. It is expected that this person will have or develop a knowledge base of the disease areas assigned and clinical research coordinator responsibilities in the clinical oncology setting.