Clinical Trials Data Coord
Competitive
HealthcareFull-time
Matthew Craven, CSM, RACRScience & PharmaceuticalPosted 30+ Days Ago
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