Research Nurse- Ambulatory Cancer

Northwell Career Site•New York, NY

About The Position

Assists in research projects involving direct patient care with adherence to established protocols so that projects are carried out as directed by the Institutional Review Board (IRB). Works within scope of practice to perform clinical procedures. Collaborates with physicians and clinical/ancillary team members to ensure integrity of research study.

Requirements

Graduate from an accredited School of Nursing.
Current License to practice as a Registered Professional Nurse in New York State required, plus specialized certifications as needed.

Nice To Haves

Bachelor’s Degree in Nursing, preferred.
Must be enrolled in an accredited BSN program within two (2) years and obtain a BSN Degree within five (5) years of job entry date.
Oncology experience preferred
Research experience preferred

Responsibilities

Participates in research project planning to determine feasibility of protocol implementation based on knowledge of institutional capabilities/limitations, therapy, and/or population of interest.
Collaborates with Principal Investigator (PI) to determine patient eligibility for clinical trial, including documentation of criteria specified in the protocol.
Ensures initial/ongoing consent process is performed and documented in compliance with the US Food and Drug Administration (FDA), Good Clinical Practice, institutional policies, sponsor requirements, Institutional Review Board (IRB) and related applicable regulations, guidelines and policies.
Participates in educating research subjects, families and healthcare team members on research study specifics and significant new information arising during conduct of trial.
Performs clinical procedures including, but not limited to, vital signs, phlebotomy, specimen collection, electrocardiograms, administration of investigational agent (under PI supervision), IV placement, catheters and patient assessment/questionnaire completion.
Participates in related audit preparation and facilitation, including FDA, IRB and related internal and external monitors and auditors.
Evaluates disease response results and physical assessment data, in conjunction with PI, to determine response per protocol.
Collaborates with PI to organize all phases of grant process for submission to funding agencies and to ensure adherence to clinical trial agreement/ study budgets.
Collaborates with PI to organize all phases of grant process for submission to funding agencies and to ensure adherence to clinical trial agreement/ study budgets.
Performs related duties as required. All responsibilities noted here are considered essential functions of the job under the Americans with Disabilities Act. Duties not mentioned here, but considered related are not essential functions.