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Registered Nurse, Oncology Research RN

Job in Newark, New Castle County, Delaware, 19711, USA
Listing for: Cooperman Barnabas Medical Center
Full Time, Part Time position
Listed on 2026-06-22
Job specializations:
  • Nursing
    Oncology Nurse, Clinical Research Nurse, RN Nurse, Nurse Practitioner
Salary/Wage Range or Industry Benchmark: 45 - 60 USD Hourly USD 45.00 60.00 HOUR
Job Description & How to Apply Below

Job Title:

Research Nurse

Location:

Cooperman Barnabas Medical Center

Department:
Cancer Center Research

Req #:

Status:
Hourly

Shift: Day

Pay Range: $45.00 - $60.00 per hour

Pay Transparency:
The above reflects the anticipated hourly wage range for this position if hired to work in New Jersey. The compensation offered to the candidate selected for the position will depend on several factors, including the candidate's educational background, skills and professional experience.

Job Overview

The Oncology Research Nurse Coordinator is a highly skilled Registered Nurse who plays a pivotal role in the execution and management of oncology clinical trials. This role blends clinical expertise with research precision—serving as the bridge between patients, physicians, and the multidisciplinary research team. From protocol activation through patient enrollment and ongoing study management, the Nurse Coordinator ensures that all clinical trials are conducted safely, ethically, and in full compliance with regulatory standards.

This position is essential in advancing cancer care through innovation while delivering compassionate, patient-centered support.

Qualifications

• Graduate of an accredited school of nursing with an active RN license in the State of New Jersey.

• Bachelor’s Degree in Nursing (BSN) preferred.

• Minimum 1 year of oncology experience required.

• 3–5 years of oncology research experience preferred.

• Current BLS (Basic Life Support) certification required.

• ONS Oncology Certified Nurse (OCN) or Advanced OCN (AOCN) preferred.

Schedule Requirements

On‑site and patient‑facing work within the standard Cancer Center hours of 7:30 am to 5:30 pm. Preference for candidates who can work 25‑30 hours/week.

Key Responsibilities

Clinical Trial Start‑Up & Protocol Activation

Collaborate with Protocol Activation teams to initiate and activate clinical trials using study start‑up workflows. Prepare and review study tools including binders, eligibility checklists, flow sheets, and patient materials. Ensure all regulatory approvals (IRB, SRB), data collection plans, and financial clearances are in place prior to activation. Analyze protocols to identify potential operational or clinical barriers and proactively resolve them with investigators.

Translate protocols into actionable clinical workflows, including treatment plans and study calendars. Provide protocol‑specific education to interdisciplinary teams.

Patient Enrollment & Study Accrual

Partner with research and clinical teams to identify and pre‑screen eligible patients for clinical trials. Review medical records to confirm eligibility and collect required source documentation. Conduct and document the informed consent process in compliance with IRB, GCP, and institutional standards. Register enrolled patients and maintain accurate documentation within clinical trial systems (e.g., OnCore).

Clinical Care & Coordination

Serve as the primary liaison between patients and the research team throughout the study lifecycle. Coordinate all protocol‑related care including appointments, diagnostics, treatments, and follow‑ups. Deliver high‑quality oncology nursing care aligned with protocol requirements and best practices. Monitor patient status, assess symptoms, and triage concerns in collaboration with the care team. Ensure accurate and timely documentation of all patient interactions and protocol visits.

Reconcile medications and communicate patient status transitions (on/off study or treatment).

Study Management & Compliance

Monitor protocol adherence and timelines; identify and elevate deviations or challenges. Accurately assess and grade adverse events using NCI criteria and protocol guidelines. Complete and submit Serious Adverse Event (SAE) reports in accordance with regulatory requirements. Support specimen collection and processing per protocol requirements. Assist with monitoring visits, audits, and sponsor communications. Contribute to Case Report Form (CRF) completion and resolution of data queries.

Maintain research records for all screened and enrolled patients.

Collaboration, Education & Professional Development

Foster strong collaboration across clinical, research,…

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