Oncology Registered Nurse (RN) – Transition to Clinical Research

Vitalief • New Brunswick, NJ

1d • $100,000 - $120,000 • Hybrid

About The Position

Vitalief is seeking an experienced Oncology Registered Nurse interested in transitioning into clinical research to support Phase II–IV oncology clinical trials at a leading research center in New Brunswick, New Jersey. The studies primarily involve investigational drugs and biologics in GI-related cancer diseases. Comprehensive on-the-job training is provided; prior clinical research experience is not required.

The nurse will work with physicians, investigators, advanced practice providers, and multidisciplinary research teams, applying oncology nursing knowledge and clinical judgment to support patient safety and clinical trial activities. The role combines patient care during assigned clinic sessions with research documentation, patient follow-up, and study coordination on non-clinic days. The position begins on-site, with one remote workday per week available after the training period.

This is full-time Vitalief employment with a Monday–Friday schedule from 8:00 AM to 4:30 PM and no nights, weekends, or holidays. The advertised annual salary is $100,000–$120,000, depending on experience and education.

Requirements

• Bachelor of Science in Nursing (BSN).
• Active Registered Nurse (RN) license in the State of New Jersey.
• At least three years of nursing experience in a hospital, outpatient, or clinic setting.
• At least one year of oncology unit nursing experience in a hospital or clinic.
• Strong clinical judgment, critical-thinking, organizational, and prioritization skills.
• Excellent communication skills and ability to explain complex clinical information in patient-friendly language.
• Ability to advocate for patient safety and adherence to clinical requirements.
• Proficiency with Microsoft Office applications, including Word, Excel, PowerPoint, Teams, and SharePoint.
• Willingness to learn clinical research systems, including OnCore™ and electronic medical records such as EPIC.
• On-site resources may be required by clients to receive annual influenza inoculation and successfully pass a Mantoux Tuberculin Skin Test (TST) for Mycobacterium Tuberculosis.

Nice To Haves

• Oncology GI experience.
• Previous clinical research experience; it is not required.

Responsibilities

• Coordinate clinical trial activities with physicians, investigators, advanced practice providers, and multidisciplinary research teams.
• Provide patient-centered oncology nursing care during clinic sessions and apply clinical judgment to support patient safety.
• Review medical records and assess patient eligibility against clinical trial criteria.
• Assist with patient identification, informed consent, enrollment, treatment coordination, and ongoing study management.
• Review treatment plans and physician orders to help ensure patient safety and adherence to study protocols.
• Coordinate patient follow-up, care activities, and research-related tasks throughout clinical trial participation.
• Review electronic medical records and source documentation to verify study requirements and maintain accurate research records.
• Support the activation and implementation of new clinical trials using OnCore™.
• Document and report Serious Adverse Events (SAEs) and maintain required study documentation in accordance with protocols and applicable regulatory requirements.
• Collaborate with clinical and research teams to support compliance with Good Clinical Practice (GCP), institutional policies, and study requirements.
• Balance clinical responsibilities during assigned clinic sessions with research documentation, patient follow-up, and study coordination on non-clinic days.

Benefits

• Healthcare coverage.
• 401(k).
• Company-paid life insurance.
• Company-paid disability insurance.
• 20 PTO days.
• Nine paid holidays.
• Comprehensive on-the-job training.
• One remote workday per week after the training period.
• Professional development and opportunity to develop clinical trial coordination, patient eligibility, research documentation, protocol compliance, and study management skills.

What This Job Offers

• Job Type: Full-time
• Career Level: Mid Level