The Clinical/Translational Study Coordinator is responsible for the organization, implementation and administration of clinical/translational research for the Department of Neurological Sciences. Provides coordination of research activities while planning, organizing and executing related daily clinical research activities (e.g. coordinator would: help evaluate research protocols for feasibility, help organize research team working on research project, lead and assist in subject recruitment, know all details of study protocol and implements study procedures as specified, coordinate subject study visits, enter any required information into Nebraska Medicine EMR, participate in data collection and completion of clinical IRB and study related research documents, including electronic data entry, assist in tracking all study visits, which may include assisting in IRB continuing renewal applications and assisting in the tracking and reconciling of research study budgets). Complies with all regulations regarding studies that involve human research participants.
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