Clinical Research Coordinator

About Us We’re Maimonides Health, Brooklyn’s largest healthcare system, serving over 250,000 patients each year through the system’s 3 hospitals, 1800 physicians and healthcare professionals, more than 80 community-based practices and outpatient centers. At Maimonides Health, our core values H.E.A.R.T drives everything we do. We uphold and maintain Honesty, Empathy, Accountability, Respect, and Teamwork to empower our talented team, engage our respective communities and adhere to Planetree's philosophy of patient-centered care. The system is anchored by Maimonides Medical Center, one of the nation’s largest independent teaching hospitals and home to centers of excellence in numerous specialties; Maimonides Midwood Community Hospital (formerly New York Community Hospital), a 130‑bed adult medical‑surgical hospital; and Maimonides Children’s Hospital, Brooklyn’s only children’s hospital and only pediatric trauma center. Maimonides' clinical programs rank among the best in the country for patient outcomes, including its Heart and Vascular Institute, Neuroscience Institute, Boneand Joint Center, and Cancer Center. Maimonides is an affiliate of Northwell Health and a major clinical training site for SUNY Downstate College of Medicine. Overview Works as research coordinator providing support necessary for the operation of ongoing clinical trials in the Department of Psychiatry. Maintains effective communication and participates in human subject research compliance activities to meet regulatory requirements. Follows established institutional policies and procedures relevant to the human subject research function. Responsibilities Assisting in study start-up operations including IRB submissions Responding to research study participant‑related inquiries Subject screening, both in‑person and virtually Infonned consent process Study subject enrollment as per inclusion and exclusion criteria Scheduling research subject in‑person and telepsychiatry visits Maintaining study logs, databases and source documents, in compliance with institutional, IRB, state and federal requirements Completing case report forms (CRFs; eCRFs) and other data collection tools as requested Handling study patient payments and reimbursements Assisting in site‑initiation and study monitoring visits Qualifications Education BS, Biological sciences or related subject. Training CITI Human Subject Research basic training Experience 2 years of Research experience in conducting investigator‑initiated and multi‑center clinical trials Pay Range USD $56,000.00 - USD $71,000.00 /Yr. Equal Employment Opportunity Employer Maimonides Medical Center (MMC) is an equal opportunity employer. #J-18808-Ljbffr