DEPARTMENT: CH - Oncology Clinical Trials.
The Coordinator Research Study is responsible for the conduction of research activities. Ensures that research is conducted in accord with the stipulations of the sponsor by working with the clinical investigators to assist in the process of enrolling patients, ordering specific tests, performing vital signs, EKGs and other assessment procedures as able within compliance to SJ/C policies, and collecting and recording data for clinical research protocols. Coordinates all components of data collection and patient enrollment in various types of patients and disease entities, which are subject of the clinical investigator, numerous protocols simultaneously ensuring assigns protocols are consistent with Good Clinical Practice (GCP), Federal Food and Drug Administration (FDA), and local organizations. Maintains open communications and is available to component organizations and practitioner sites for consultation.
RN in the State of Georgia is required. 2-3 years of Clinical Research within Oncology is preferred. Oncology experience preferred. Professional License with State of Practice is required. National certification in current specialty within 18 months of hire upon eligibility.