Oncology Nurse (RN) - Clinical Research Career Opportunity

Vitalief

• $100K — $120K *
Healthcare
Less than 5 years of experience
Job Overview by Ladders

Qualifications

  • Bachelor of Science in Nursing (BSN) required.
  • Active Registered Nurse (RN) license in New Jersey.
  • Minimum 3 years nursing experience in hospital or outpatient settings.
  • At least 1 year oncology nursing experience in a hospital or clinic setting.
  • Experience in clinical research is a plus but not required.
  • Strong critical thinking and prioritization skills.
  • Excellent communication skills for patient and team interactions.

Responsibilities

  • Coordinate and support Phase II-IV Medical Oncology clinical trials under the direction of the Study Site Leader.
  • Provide exceptional patient-centered oncology nursing care and coordinate protocol-related activities.
  • Collaborate with research teams to prepare, initiate, and conduct clinical trials, including patient enrollment and treatment coordination.
  • Ensure patient safety and protocol compliance through clinical judgment and accurate documentation.
  • Support physician practices with direct patient care and research activities during clinic schedules.
  • Facilitate activation and implementation of new clinical trials with the Protocol Activation Office.
  • Review electronic medical records to verify protocol eligibility and maintain accurate research documentation.

Benefits

  • Comprehensive benefits package including health and wellness coverage.
  • On-the-job training in clinical trials for skill development.
  • Opportunities for career advancement in clinical research.
  • Collaborative work environment with multidisciplinary teams.
  • Engagement with leading medical centers and research institutions.
Full Job Description
THE ROLE
We are seeking an experienced Oncology Nurse to join our team as a full-time Vitalief employee (with a comprehensive benefits package) supporting interventional oncology clinical trials across multiple disease areas at a leading research center in New Brunswick, NJ.

This is an excellent opportunity for a registered nurse (RN) with oncology experience to transition into a fulfilling career in clinical research and contribute to oncology studies. Comprehensive on-the-job training in clinical trials will be provided.

RESPONSIBILITIES:
  • Under the direction of the Clinical Research Study Site Leader, coordinate and support Phase II-IV Medical Oncology clinical trials, primarily involving investigational drugs and biologics, with limited device, radiation oncology, and surgical oncology studies.
  • Provide exceptional, patient-centered oncology nursing care while coordinating protocol-related activities with investigators, physicians, advanced practice providers, and multidisciplinary teams in accordance with study protocols, Good Clinical Practice (GCP), institutional policies, and regulatory requirements.
  • Collaborate with investigators and research teams to prepare, initiate, and conduct clinical trials, including patient identification, eligibility assessment, informed consent, enrollment, treatment coordination, and ongoing protocol management.
  • Apply strong clinical judgment and critical thinking to ensure patient safety, protocol compliance, accurate documentation, and appropriate review of treatment plans and physician orders throughout study participation.
  • Support assigned physician practices based on clinic schedules by providing direct patient care during clinic sessions and completing research-related activities on non-clinic days, including documentation, patient follow-up, order review, care coordination, and study management.
  • Partner with the Protocol Activation Office to facilitate the successful activation and implementation of new clinical trials using the OnCore™ Clinical Trials Management System (CTMS).
  • Review electronic medical records and source documentation to determine protocol eligibility, verify study requirements, and maintain complete and accurate research documentation.
  • Perform essential clinical research responsibilities, including documenting and reporting Serious Adverse Events (SAEs), maintaining study records within OnCore™ and the electronic medical record, preparing patient study calendars, and ensuring compliance with institutional, sponsor, and federal regulatory requirements.

REQUIRED SKILLS:
  • Bachelor of Science in Nursing (BSN) required.
  • Active Registered Nurse (RN) license in the State of New Jersey.
  • Minimum 3 years of nursing experience in a hospital setting or outpatient or clinic setting.
  • At least 1 year of oncology nursing experience working within an oncology unit in a hospital or clinic setting.
  • Some experience in a clinical research or trial participant-facing role is a plus but not required (training will be provided).
  • Strong critical thinking and prioritization skills, with the confidence to be appropriately assertive in advocating for protocol adherence and patient safety.
  • Excellent communication skills: serve as a key liaison across departments and effectively translate complex clinical information into clear, patient-friendly language.
  • Proficiency in document and data management tools, including Microsoft Word, Excel, PowerPoint, Adobe, Teams, and SharePoint.
  • Detail-oriented, proactive, and adaptable, with the ability to thrive in a fast-paced, academic, and diverse environment.
  • Comfortable learning and using clinical systems such as OnCore™, electronic medical records (i.e. EPIC), and other clinical trial management tools.

PHYSICAL DEMANDS: Standing, sitting, walking, visual perception, talking and hearing. Lifting up to 20lbs.

IMPORTANT NOTE:Vitalief partners with clients such as major medical centers and academic institutions that often requires all on-site resources such as prospective Vitalief consultants to be inoculated annually for Influenza and successfully pass a Mantoux Tuberculin Skin Test (TST) for Mycobacterium Tuberculosis.

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