The Research Regulatory Coordinator assists with the daily regulatory maintenance and compliance of clinical research studies at ECU and ECU Health. The coordinator works closely with study sponsors, clinical units, research teams, the UMCIRB office, and external IRBs, managing a portfolio of studies across the enterprise and supporting investigators and clinical and research staff with required regulatory activities. The role assists with preparing required documents, maintaining study and participant records, supporting regulatory workflows, and conducting compliance auditing. The coordinator works independently and as part of the research team to maintain trackers and quality controls for informed consent, protocol deviations, amendments, and other essential regulatory functions. This is a hybrid position.
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Job Type
Full-time
Career Level
Entry Level