Research Nurse-Ambulatory Oncology

Northwell

New Hyde Park, NYFull-timePosted Mar 19, 2026

Behavioral Health Market Context

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Job Description

ates 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.

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

Nice-to-haves
• Research experience preferred
• Oncology experience preferred

Qualifications

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

Benefits

    Responsibilities

    • 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
    • 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
    • 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


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