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Responsibilities Data abstraction CRF completion Query resolution Sponsor monitor visit coordination Maintaining audit-ready data Oversee electronic research records and patient information in the CTMS Possess in-depth knowledge of Good Clinical Practices (GCP), Food and Drug Administration (FDA) regulations, NIH guidelines, and HIPPA regulations Collaborate effectively as a valuable member of the clinical research t

Responsibilities Possess in-depth knowledge of Good Clinical Practices (GCP), Food and Drug Administration (FDA) regulations, NIH guidelines, and HIPPA regulations Collaborate effectively as a valuable member of the clinical research team, demonstrating clear and timely written and verbal communication skills, including the sharing of critical information Take responsibility for communicating any protocol deviations