Clinical Research Coordinator

Overview Clinical Research Coordinator II (CRC II) – New York City Area. Full-Time, Hourly + Benefits. We’re hiring an experienced Clinical Research Coordinator II (CRC II) to independently manage complex and high-enrolling clinical trials at a growing research site in the NYC area. This role is ideal for a coordinator who has moved beyond entry-level responsibilities and is ready to own studies end-to-end , serve as a key sponsor-facing contact, and help drive enrollment, data quality, and inspection readiness. What You’ll Do Independently manage a portfolio of complex and/or high-volume clinical trials Fully own study execution including screening, enrollment metrics, and visit conduct Conduct all participant visits, clinical procedures, and eligibility assessments per protocol Lead study start-up activities (SIV prep, regulatory readiness, supplies, staff training support) Serve as the primary liaison with sponsors, monitors, and CROs Oversee source documentation, data entry, and query resolution Maintain full investigational product (IP) accountability and compliance Identify operational risks and recommend corrective actions Compile and present study metrics to internal leadership and sponsor partners Train and oversee CRC Is or Research Assistants supporting your studies What We’re Looking For 1+ year of clinical research experience (industry-sponsored trials required) Background in Psychiatry, Neurology, Mental Health Demonstrated ability to manage trials independently Strong protocol comprehension and clinical skills Comfortable communicating directly with sponsors and CROs Highly organized, proactive, and quality-driven Why This Role Clear ownership and autonomy Exposure to complex, sponsor-facing trials Growth path toward CRC III / site leadership Competitive hourly pay + full benefits How to Apply Interested or know someone great? Apply directly on LinkedIn or message me to discuss details confidentially. #J-18808-Ljbffr