Advanced Practice Oncology Researcher, Early Phase

The START Center for Cancer Research; East Brunswick Township (NJ); On-site; USD 170,000 - 195,000; Full time

Job summary

The START Center for Cancer Research is seeking an Advanced Practice Provider to support protocol-driven care in Phase I and other early-phase oncology studies. You will function as a sub-investigator under the supervision of the Principal Investigator to extend clinical capacity and ensure study quality.

Responsibilities include conducting physical examinations, coordinating visits, reviewing histories, assisting with screening and adverse event documentation, and collaborating with nursing,

Qualifications

• Advanced practice degree and current licensure in the applicable state(s).
• Minimum of 5 years of oncology clinical care or oncology clinical research experience.
• Preferred: master's or doctoral degree in APRN/PA studies; national certification; eligibility to serve as sub-investigator; prior early-phase oncology research.

Responsibilities

• Serve as a sub-investigator on assigned early-phase clinical trials under PI supervision.
• Conduct protocol-required physical examinations and study visits for screening, on treatment, and follow-up as delegated by the PI.
• Prepare comprehensive medical histories and clinical summaries for new patient consults.
• Assist with screening activities before new patient visits, including chart review and protocol feasibility.
• Support post-consent screening with protocol-specific screening questions and clarifications.
• Identify, document, and follow up on adverse events in collaboration with the PI and research team.
• Coordinate with nursing, pharmacy, CRAs, and data management to ensure safe, protocol-adherent care.

Education

Advanced practice degree (NP or PA)

Current state licensure

Master's or Doctoral degree in advanced practice nursing or physician assistant studies

Job description

The START Center for Cancer Research is seeking an Advanced Practice Provider to support protocol-driven care in Phase I and other early-phase oncology studies. You will function as a sub-investigator under the supervision of the Principal Investigator to extend clinical capacity and ensure study quality.

Responsibilities include conducting physical examinations, coordinating visits, reviewing histories, assisting with screening and adverse event documentation, and collaborating with nursing,