New

Clinical Research Coordinator (CHIME) - Endocrinology (NYNORC)

Columbia University
United States, New York, New York
Feb 24, 2026
Job Type: Officer of Administration Regular/Temporary: Regular Hours Per Week: 35 Salary Range: $66,300 - $66,300 The salary of the finalist selected for this role will be set based on a variety of factors, including but not limited to departmental budgets, qualifications, experience, education, licenses, specialty, and training. The above hiring range represents the University's good faith and reasonable estimate of the range of possible compensation at the time of posting. Position Summary The Comparing Health Interventions for Maternal Equity (CHIME) Trial is seeking a fulltime Clinical Research Coordinator to support study operations within the New York Nutrition Obesity Research Center (NYNORC) at Columbia University Medical Center. The NYNORC is dedicated to excellence in clinical, translational, and basic research, advancing scientific discovery through interdisciplinary collaboration. The Clinical Research Coordinator will work under the direction of the Principal Investigator and study team to assist with the daytoday coordination of study activities at CUIMC. Training will be provided. Responsibilities Assist the Principal Investigator and study team with the implementation and maintenance of study protocols. Support the organization and scheduling of study visits and required procedures. Conduct participant outreach, including collaboration with OBGYN Recruitment staff. Obtain informed consent and screen prospective participants for eligibility. Perform weekly EHR reviews to identify potential participants and request provider permission to approach patients. Conduct data collection per protocol and perform timely, accurate data entry. Maintain communication with the Data Coordinating Center to ensure data completeness and quality. Create and maintain participant binders and other required study documentation, including recruitment and incidence logs. Maintain ongoing contact with enrolled participants to support retention and adherence to study procedures. Prepare study materials, manage study correspondence, and assist with regulatory and documentation tasks as directed. Attend weekly study meetings, virtual/inperson Steering Committee meetings, and Coordinator calls, presenting updates as needed. Assist with study-related procedures following completion of required training and certification. Perform other related duties as assigned. Minimum Qualifications Bachelor's degree or equivalent in education, training, and experience. Knowledge of human physiology, biology, and/or nutrition. Strong organizational and communication skills. Ability to present and relay information clearly to investigators and study staff. Computer proficiency and prior experience with data collection. Ability to troubleshoot issues and apply basic technical problemsolving skills. Bilingual/fluent in Spanish and English. Ability to perform light physical activity. Availability for occasional weekend procedures. Preferred Qualifications Bachelor's degree in nutrition, science, or a healthrelated field. 1-3 years of related research experience. Experience with data collection and basic data management. Knowledge of human physiology, biology, and/or nutrition. Other Requirements Medical clearance and participation in the medical surveillance program Contact with patients and/or human research subjects Potential bloodborne pathogen exposure Successful completion of applicable compliance and systems training requirements Equal Opportunity Employer / Disability / Veteran Columbia University is committed to the hiring of qualified local residents.