The Clinical Research Nurse Coordinator, under the guidance and supervision of the Principal Investigator (PI) and Clinical Research Nurse Manager, ensures the integrity and quality of clinical trials are maintained and conducted in accordance w/ federal, state, and local regulations, Institutional Review Board (IRB) approvals, and Holy Name policies and procedures. Experience in non-human-subjects research, quality improvement, or public health research is valuable, but these experiences alone do not necessarily translate to coordinating FDA-regulated clinical trials involving active participants, protocol-driven visits, safety reporting, regulatory documentation, and enrollment expectations.