Clinical Research Coordinator III

The Trustees of Columbia University in the City of New York • New York, NY • 1h ago

Job Type: Officer of Administration Bargaining Unit: Regular/Temporary: Regular End Date if Temporary: Hours Per Week: 35 Standard Work Schedule: Building: Salary Range: $75,000 - $82,000The 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 SummaryColumbia University Irving Medical Center (CUIMC) provides global leadership in scientific research, health and medical education, and patient care. Home to approximately 4,472 students and over 3,000 part-time and full-time faculty members, the health sciences campus includes the four professional schools-the Vagelos College of Physicians and Surgeons, the College of Dental Medicine, the School of Nursing, and the Mailman School of Public Health.Our staff is pivotal in facilitating and advancing these cutting-edge research endeavors. Working in the Department of Obstetrics and Gynecology the CRC III will support the coordination of clinical research activities according to clinical research studies or trials managed by the Department. The CRC III works with complex trials/clinical studies, serves as a mentor as applicable, and is responsible for day-to-day study monitoring activities. They will also be responsible for the coordination of patient participation (including screening, recruitment, assessment, and follow-up of study participants), collection and maintenance of study data, ensuring adherence to study activities as described in the protocol, and working with other members of the research team to coordinate all other aspects related to the conduct of the clinical trial or study. The individual will monitor and support all administrative items of the research portfolio and support the NICHD-sponsored Stillbirth Network grant, the Complex Contraceptive Trial Network grant and the Global Network grant. A research background is highly preferred.ResponsibilitiesClinical Trials Coordination Serving as the lead CRC, they are responsible for day-to-date aspects of study protocol tasks including participant recruitment, screening, enrollment and follow-up with study participants, specimen processing, and other key protocol elements. Effectively communicate, verbally and written, build and maintain relationships with potential study subjects, participants, clinicians, and other health care providers, and reach office staff to support the successful administration of clinical trials/studies. Design recruitment and retention plans for a range of different study populations utilizing different modes of communication. Recruit and enroll for Network studies as assigned following all regulatory procedures. Complete data entry activities, including Protected Health Information (PHI), clinical, billing, and other administrative data with minimal supervision and summarize and assist in analyzing operational data for the research team. Coordinate day-to-day aspects of study relayed procedures, samples, documentation, and visit management. Carry out required staff training and provide the direct supervision for assigned staff. Maintain accurate and complete clinical research files which may include administering questionnaires, completing case report forms (CRFs), completing any study start-up or close-out documentation. Implement the study start up and site initiation visit (SVI). Coordinate fiscal transactions related to the study including compensation to study subjects for their participation and helping them troubleshoot any issues. Adhere to workplace and patient safety protocols, monitor area to ensure compliance with ethical and safety standards for research. Coordinate and manage

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