Clinical Research Coordinator (CRC) - Bronx, NY

Clinical Research Coordinator (CRC) Position Summary Mon-Fri, Flexible Schedule Oversight of ~3 Study Sites The Clinical Research Coordinator (CRC) is responsible for the day-to-day coordination and operational execution of clinical trials conducted within outpatient healthcare settings. The CRC ensures that clinical trials are conducted in accordance with: ICH Good Clinical Practice (GCP) FDA regulations Institutional Review Board (IRB) requirements Sponsor protocols Internal Standard Operating Procedures (SOPs) The CRC serves as the primary operational liaison between study participants, the Principal Investigator (PI), sponsors or Contract Research Organizations (CROs), and internal leadership. The role focuses on ensuring patient safety, regulatory compliance, data integrity, and successful study execution. Reporting Structure The Clinical Research Coordinator reports to operational leadership within the research program. Clinical oversight is provided by the Site Principal Investigator (PI). Study Start-Up and Site Preparation Assist with the preparation and activation of clinical trials at assigned healthcare sites. Responsibilities include: Reviewing study protocols and investigator brochures Assisting with site feasibility assessments Preparing regulatory binders and study documentation Coordinating site initiation visits Ensuring required equipment and study supplies are available Assisting with IRB submissions and regulatory documentation Coordinating staff protocol training Participant Recruitment and Screening Identify and recruit eligible study participants from t