Clinical Research Coordinator

Equity Medical is actively seeking an experienced Clinical Research Coordinator to join our growing New York research team at our Bronx or Manhattan sites. Equity Medical is a rapidly expanding multi‑site clinical research organization conducting Phase I‑IV clinical trials across multiple therapeutic areas including dermatology, allergy/immunology, respiratory, rheumatology, neurology, and metabolic diseases. Our mission is to bring innovative treatment options to underserved communities through high‑quality, compliant, and patient‑centered clinical research operations. We are looking for a highly motivated and experienced Clinical Research Coordinator with prior experience managing interventional pharmaceutical‑sponsored clinical trials. This is not an entry‑level opportunity. The ideal candidate will be comfortable working independently in a fast‑paced clinical research environment and capable of managing study responsibilities while collaborating closely with investigators, sponsors, CROs, and site leadership. Locations: Bronx, NY Manhattan, NY Key Responsibilities: Coordinate and oversee all aspects of assigned clinical trials from startup through closeout Conduct study visits, patient scheduling, informed consent, and source documentation Ensure protocol compliance, GCP adherence, and regulatory compliance Recruit and screen potential study participants Maintain accurate and audit‑ready regulatory and study documentation Communicate directly with sponsors, CROs, monitors, investigators, and study participants Support monitoring visits, sponsor communication, and site operations Assist with study startup activities and regulatory submissions Enter and maintain accurate data within sponsor and clinical trial systems Qualifications: Bachelor’s degree or equivalent combination of education and experience Minimum of 3 years of clinical research coordination experience preferred Prior experience with interventional pharmaceutical‑sponsored clinical trials required Strong understanding of GCP, FDA regulations, and clinical trial workflows Experience independently managing multiple studies simultaneously Excellent organizational, communication, and problem‑solving skills Strong attention to detail and ability to thrive in a growing organization Other Requirements: Completion of applicable compliance and systems training requirements All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, pregnancy, national origin, age, disability, genetic information, veteran status, sexual orientation, gender identity, or any other protected characteristic under applicable federal or state law. #J-18808-Ljbffr