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Nurse Practitioner

Job in New York, New York County, New York, 10261, USA
Listing for: Columbia University
Full Time position
Listed on 2026-06-05
Job specializations:
  • Nursing
    Nurse Practitioner
Salary/Wage Range or Industry Benchmark: 100000 - 140000 USD Yearly USD 100000.00 140000.00 YEAR
Job Description & How to Apply Below
Location: New York

  • Job Type: Officer of Administration
  • Bargaining Unit:
  • Regular/Temporary:
    Regular
  • End Date if Temporary:
  • Hours Per Week: 35
  • Standard

    Work Schedule:
  • Building:
  • Salary Range: $100,000 - $140,000

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 Division of Pediatric Hematology, Oncology, and Stem Cell Transplant at Columbia Children’s Health, New York-Presbyterian Morgan Stanley Children’s Hospital (MSCH) is one of the oldest and most comprehensive centers in the country focused on treating children with cancer and blood disorders. MSCH has 202 inpatient pediatric beds, including a 54-bed Pediatric Intensive Care Unit and 10 operating rooms. Our division is currently composed of 3 sections (Hematology, Oncology and Stem Cell Transplantation) with 22 full-time faculty, 3 research RN/NP’s, 8 clinical research associates, and 3 regulatory specialists and includes an ACGME-accredited Fellowship Program and a FACT-accredited stem cell transplant program.

We are seeking a Nurse Practitioner to work in the Research Capacity to join our team in a full-time position within Oncology for Clinical Research focused on working on the Immuno-Oncology Program (PIRD).

Responsibilities
  • Responsible for the coordination, oversight and administration of clinical research protocols.
  • NP will be responsible for screening prospective study participants.
  • Take comprehensive history and perform physical examinations.
  • Conduct informed consent discussions and obtain consent.
  • Attend and/or perform all protocol required visits either independently or as a shared visit depending on treating physician’s preference. Initial or restaging assessment visits must be performed with the treating physician.
  • Order and interpret radiology, laboratory, and diagnostic tests as appropriate.
  • Prescribe and manage supportive care medications.
  • Perform phone triage for acute clinical issues and conduct phone assessments as required per protocol and prescribe treatment as needed
  • Instructing participants about use of study products or drugs.
  • Verify Study drug/Standard of Care orders if entered by another Physician Investigator/Fellow/NP.
  • Obtain pre-certifications and prior authorizations for procedures / prescriptions when requested.
  • Create and provide protocol-related in-services for both inpatient and outpatient Nursing Staff.
  • Completing case report forms.
  • Filing serious adverse event reports and working with Clinical Research Coordinators to identify and classify serious adverse events.
  • Developing and overseeing a quality management plan. Oversees data reporting requirements to ensure consistent integration with existing institutional frameworks, including timely and accurate submission to CIBMTR and other designated data repositories. Ensures high-quality clinical trial data capture and reporting in alignment with operational standards and program expectation. Monitors clinical trial and treatment fidelity across sites of care, proactively identifying barriers to implementation and leading process improvement efforts.
  • Preparation of regulatory documents for IRB submission.
  • Self-directed review of new protocols, and reeducation on existing protocols.
  • Serve as a liaison between PI’s and study sponsors in both outpatient and inpatient areas;
  • Serves as a liaison with pharmacy and research pharmacy
  • Serves as subject matter expert in the planning and clinical execution of new cellular immunotherapy program and clinical trials.
  • Leads the design and operationalization of care pathways, workflows, and clinical infrastructure to support safe and effective delivery of cellular immunotherapy, with a focus on CAR T cell therapy.
  • Partners with physicians, clinical trial investigators, research teams, pharmacy, cell lab, apheresis, and hospital administration to ensure seamless coordination across all care and research touchpoints.
  • Functions as the central…
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