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Columbia University Irving Medical Center is seeking an Oncology Research Nurse to support oncology clinical research in White Plains, NY. This full-time, on-site role involves coordinating protocols, screening patients, obtaining consent, and conducting study visits.
You will administer treatments per protocol, document data accurately, and ensure regulatory compliance while collaborating with physicians, coordinators, and care teams. Requires NYS RN licensure and BSN.
Columbia University Irving Medical Center (CUIMC) is a leading clinical, research, and educational institution located in northern Manhattan, home to four professional schools focused on advancing health sciences and patient care. Through the Vagelos College of Physicians and Surgeons, College of Dental Medicine, School of Nursing, and Mailman School of Public Health, CUIMC provides global leadership in scientific discovery and medical education. The medical center delivers comprehensive general and specialized medical, dental, and nursing services across the New York City metro area, supported by more than 1,800 clinicians. CUIMC is recognized for combining innovative, evidence-based treatments with compassionate care for patients and families. The organization is dedicated to maintaining the highest standards of quality, safety, and clinical excellence.
The Oncology Research Nurse is a full-time, on-site role located in White Plains, NY, supporting oncology clinical research activities within CUIMC’s patient care and research programs. This role is responsible for coordinating and implementing oncology research protocols, including patient screening, enrollment, informed consent, and ongoing study visits. Day-to-day responsibilities include administering treatments and interventions per protocol, monitoring patient status, documenting clinical and research data accurately, and ensuring adherence to regulatory and ethical standards. The Oncology Research Nurse collaborates closely with physicians, research coordinators, and multidisciplinary care teams to support study design, data collection, and patient safety. The role also involves patient and family education about clinical trials, participation requirements, and available support resources.