Oncology Registered Nurse; RN Transition to Clinical Research

Ready to Take Your Oncology Nursing Career in a New Direction? Bring your oncology nursing experience into clinical research - with comprehensive training and no prior research experience required!

Vitalief is seeking an experienced Oncology Registered Nurse (RN) interested in transitioning into clinical research to support oncology clinical trials at a leading research center in New Brunswick, NJ.

This is an excellent opportunity to build a new professional specialty while continuing to use your clinical knowledge, critical-thinking skills, and passion for patient care. You'll work alongside physicians, investigators, and multidisciplinary research teams supporting clinical trials that evaluate innovative cancer treatments and contribute to the advancement of cancer care.

If you're looking for a new challenge, a predictable weekday schedule, and an opportunity to expand your nursing career beyond traditional bedside care, we'd love to hear from you.

• No Clinical Research Experience
  
  Required:
  
  Comprehensive on-the-job training will be provided to help you transition into clinical research.
• Competitive Salary: Earn $100,000–$120,000 annually, depending on experience and education.
• Work-Life Balance: Enjoy a Monday–Friday schedule, 8:00 AM–4:30 PM, with no nights, weekends, or holidays.
• Hybrid Flexibility: Begin on-site in New Brunswick, NJ, with one remote workday per week after the training period.
• Continue Making a Difference in Oncology: Apply your nursing expertise to clinical trials evaluating investigational cancer therapies.
• Professional Growth: Develop valuable new skills in clinical trial coordination, patient eligibility, research documentation, protocol compliance, and study management.
• Comprehensive Benefits: Healthcare coverage, 401(k), company-paid life and disability insurance, 20 PTO days, and nine paid holidays.
• Full-Time Vitalief Employment: Join a clinical research-focused organization that values its employees and supports professional development.

• Working under the direction of the Clinical Research Study Site Leader, you'll support Phase II–IV oncology clinical trials, primarily involving investigational drugs and biologics within GI-related cancer diseases.
• 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™, a clinical trial management system.
• 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.
• You'll balance clinical responsibilities during assigned clinic sessions with research documentation, patient follow-up, and study coordination activities on non-clinic days.

• Bachelor of Science in Nursing (BSN).
• Active Registered…