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Clinical Research Coordinator - Endocrinology

Columbia University
United States, New York, New York
May 03, 2025
Job Type: Officer of Administration Regular/Temporary: Regular Hours Per Week: 35 Salary Range: $64,350 - $64,350 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 Working closely with the Principal Investigator, the Clinical Research Coordinator will assist in all aspects of human physiologic studies in the field of type 2 diabetes and non-alcoholic fatty liver disease. We are seeking a Clinical Research Coordinator to assist in all aspects of human physiologic studies in the field of type 2 diabetes and non-alcoholic fatty liver disease. The CRC will work closely with the Principal Investigator to assist in the coordination of tests/visits for research participants, interface with vendors and collaborating services, ensure regulatory compliance, and curate and enter study data. The Candidate should be motivated, excited to play a crucial role in research, and willing to exercise independent judgment within the scope of the research in order to meet expected goals. Enter details here Responsibilities Assist with the day-to-day general operation of clinical research projects. Screen participants, recruit/retain participants, and schedule and organize study visits. Assist with the conduct of study procedures. Educate participants regarding study procedures, logistics, and other pertinent information. Coordinate reimbursements/compensation for study participants. Coordinate of tests/visits for research participants. Responsible for data collection and entry; maintain study database, and ensure data accuracy. Monitor data (including safety data) on case report forms. Ensure compliance with the study protocol and all relevant research regulations. Interact with centralized research resources such as the Institutional Review Board (IRB), the Clinical Research Center (CTSA-CRR), the Clinical Trials Office (CTO), and other regulatory bodies. Responsible for inventory and procurement of supplies, including contact with vendors, proper storage, and keeping up-to-date logs. Assist with publications, various grant reports, and agency reporting including NIH Data Safety Monitoring: generate graphs, figures, tables, and organize references with EndNote. Perform additional related duties as needed. Minimum Qualifications Bachelor's degree or equivalent in education, training, and experience, plus two years of related experience Basic computer skills including Microsoft Office Strong verbal and written communication skills Careful attention to detail Ability to work independently, developing and exercising professional judgment, and thinking creatively to work through problems Excited to engage in all aspects of scientific research involving human participants Preferred Qualifications Proficiency in Spanish and/or willingness to use phone interpreter service Prior experience working with patients and/or human participants under HIPAA and GCP Working knowledge of electronic research tools such as Epic (electronic health record) and/or Clinical Trial Management Systems Other Requirements Participation in the medical surveillance program Potential bloodborne pathogen exposure Contact with patients and/or human research participants 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.