Clinical Research Coordinator

This role involves independently managing industry-sponsored interventional clinical trials from site initiation through close-out, coordinating multiple concurrent studies, and supporting investigators with study-related tasks. The position requires screening and enrolling participants, managing data and monitoring visits, and maintaining regulatory compliance and quality assurance. The coordinator serves as the primary point of contact for sponsors, CRAs, and participants while ensuring adherence to ICH-GCP, FDA regulations, and HIPAA standards.