Parsippany, New Jersey2 days ago
The incumbent may work closely with internal including Clinical Operations, Data Management, Statistics, Regulatory Affairs, Pharmacovigilance, Scientific Communications, and Executive staff, as well as external consultants, clinical research organizations (CROs), vendors, and clinical site personnel. Performance Monitoring: In collaboration with the Clinical Trial Manager (CTM) and site Clinical Research Associate (CRA), evaluate study protocols for enrollment risks, monitor site metrics, and implement mitigation plans to maintain timelines.