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Oncology APP​/NP

Job in Fort Worth, Tarrant County, Texas, 76102, USA
Listing for: START Center for Cancer Research
Full Time position
Listed on 2026-08-29
Job specializations:
  • Nursing
    Oncology Nurse, Nurse Practitioner, Clinical Research Nurse
Salary/Wage Range or Industry Benchmark: 120000 - 165000 USD Yearly USD 120000.00 165000.00 YEAR
Job Description & How to Apply Below

The START Center for Cancer Research (“START”) is the world’s largest early phasesite network, fully dedicated tooncologyclinical research.

Throughout our history, START has provided hope to cancer patients inglobalcommunity practices by offering"Hope Through Access”tocutting edge trials throughout the United Statesand Europe.

We are seeking an Advanced Practice Provider / Nurse Practitioner.

This role supports protocol-compliant patient care and clinical trial execution for Phase I and other early-phase oncology studies. Functioning as a sub-investigator under the supervision of the Principal Investigator (PI), the APP/NP extends clinical capacity, supports screening and study visits, and enhances care coordination while preserving core investigator responsibilities specific to early-phase research.

Work Schedule:

Monday-Friday, 8:00am-5:00pm

Location:

900 W. Magnolia Ave,Suite 200,Fort Worth, Texas 76104

Essential Responsibilities:
  • Serve as a sub-investigator on assigned early-phase clinical trials following completion of required training and delegation documentation.
  • Conduct protocol-required physical examinations and study visits for patients in screening, on treatment, and in follow-up as delegated by the Principal Investigator.
  • Prepare comprehensive medical histories and clinical summaries in advance of new patient consults to support efficient PI evaluation.
  • Assist with screening activities prior to new patient visits, including preliminary chart review and protocol feasibility assessment.
  • Support post-consent screening by assisting with protocol-specific screening questions and required clarifications.
  • Assist with the identification, documentation, and follow-up of adverse events (AEs) and serious adverse events (SAEs) in collaboration with the Principal Investigator and research team. Attend sponsor or safety calls designated as low priority or routine, as delegated by the Principal Investigator.
  • Act as the first point of clinical contact for the research care team for day-to-day patient management questions and elevate issues to the Principal Investigator as appropriate.
  • Coordinate with nursing, pharmacy, clinical research coordinators, and data management to ensure safe, efficient, and protocol-adherent care delivery.
Required

Education and Experience:
  • Advanced practice degree (Nurse Practitioner or Physician Assistant) with current licensure in the applicable state(s).
  • Minimum of 5 years of experience in oncology clinical care or oncology clinical research.
Preferred

Education and Experience:
  • Master’s degree or Doctoral degree in advanced practice nursing or physician assistant studies.
  • National certification as a Nurse Practitioner or Physician Assistant. Eligibility and willingness to serve as a sub-investigator on oncology clinical trials.
  • Prior experience in early-phase (Phase I) oncology clinical research.
More About START

START clinical trial sites have conducted more than 1,000 early-phase clinical trials, including dozens of therapies that were approved by the FDA or EMA. STARTrepresentsthe world’s largest roster of early-phase principal investigators across its Network of clinical trial sites. Committed to accelerating passage from trials to treatments, START delivers hope to patients, families, and physicians around the world via our mission of “Hope Through Access”.

Learn more at

Ready to be part of a team changing the future of cancer treatment?

We are an equal opportunity employer that welcomes and encourages diversity in the workplace. We do not discriminate on the basis of race, color, religion, marital status, age, national origin, ancestry, physical or mental disability, medical condition, pregnancy, genetic information, gender, sexual orientation, gender identity or expression, veteran status, or any other status protected under federal, state, or local law.

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