Clinical Research Nurse (RN) - Oncology
Vitalief is a clinical research consulting organization that partners with leading academic and hospital-based research centers to accelerate study timelines, optimize operations, and improve patient outcomes. We are seeking a Clinical Research Nurse (RN) to support high-priority Phase II–III oncology trials at a respected outpatient cancer center in Somerville, NJ. THE ROLE
This is an outstanding opportunity for an experienced RN ready to transition into clinical research. You’ll receive comprehensive, hands-on training in oncology and clinical trial operations while working alongside physicians and research leaders at the forefront of cancer care. WHY VITALIEF?
- Contribute to advancing scientific discoveries: that improve patient lives.
- PEOPLE FIRST culture: with opportunities for growth and innovation.
- Competitive benefits : include 20 PTO days + 9 paid holidays; Company-paid life insurance and short/long-term disability; 401(k) retirement program; Comprehensive healthcare plans.
- Work schedule: 5 days (Monday to Friday) per week on-site (Somerville, NJ) initially; then 4 days on-site and 1 day remote weekly after the training period.
- Standard work hours: 8:00am to 4:30pm.
- Market-competitive salary : commensurate with experience.
Support Phase II–III interventional Medical Oncology trials under the Clinical Research Director, delivering protocol-driven, compassionate oncology nursing care in alignment with GCP. Act as a high-autonomy clinical partner, ensuring patient safety, protocol compliance, and collaboration with investigators and ancillary teams. Balance clinic-based direct patient care with non-clinic documentation, follow-up, and coordination. Screening & Enrollment (50%)
- Screen 750–900 patients monthly across 40–50 trials using clinic schedules, pathology reports, MDCs, and referrals.
- Conduct eligibility assessments, review records/pathology, secure source documentation, and coordinate informed consent with investigators.
- Manage patients from consent through treatment completion, ensuring protocol adherence and safety.
- Maintain regulatory files, subject binders, and study documentation.
- Perform core research tasks (SAE reporting, record maintenance, OnCore™ access, study calendar prep) and transition patients to CTS/CRC teams for long-term follow-up.
- Graduate of an accredited nursing program with an active New Jersey RN license.
- BSN required.
- Minimum 3 years of nursing experience (hospital or outpatient setting).
- Oncology and/or clinical trial experience preferred – but NOT REQUIRED!
- Strong critical thinking, prioritization, and assertiveness in advocating for protocol adherence and patient safety.
- Excellent communication skills with the ability to collaborate across departments and translate complex clinical information for patients.
- Proficient in Microsoft Office (Word, Excel, PowerPoint), Adobe, Teams, and SharePoint.
- Detail-oriented, proactive, adaptable, and comfortable working in a fast-paced academic environment.
- Ability to learn and effectively use OnCore™, EMRs, and other clinical trial management systems.
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