Tandem Intermediate LLC
Somers Point, NJ
Clinical Research Coordinator (CRC) The Clinical Research Coordinator (CRC) is responsible for overseeing and managing the daily operational activities of assigned clinical research studies. This role works closely with investigators, clinical staff, study participants, sponsors, and CROs to ensure that all research activities are conducted in compliance with study protocols, regulatory requirements, and ethical standards. The CRC serves as the primary owner of study coordination, documentation, data management, and sponsor communication, supporting compliant trial execution from study start-up through close-out. Key Responsibilities Study Management & Coordination Organize, plan, and coordinate all aspects of assigned clinical trials from initiation through close-out. Support study start-up activities including feasibility, regulatory submissions, and site activation. Attend investigator meetings, site initiation visits, and other study-related meetings. Manage visit...