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Research Nurse

Job in California, Moniteau County, Missouri, 65018, USA
Listing for: Stanford University
Full Time position
Listed on 2025-12-02
Job specializations:
  • Healthcare
    Clinical Research
  • Research/Development
    Clinical Research
Job Description & How to Apply Below
Position: Research Nurse 2
Location: California

Thank you for your interest in Stanford University. While we have instituted a hiring pause for non‑critical staff positions, we are actively recruiting for most of the positions currently listed on our careers page. We will update the page when the broader hiring pause is lifted.

Job Summary
  • DATE POSTED 3 days ago
  • Schedule Full‑time
  • Job Code 4592
  • Employee Status Regular
  • Grade K
  • Requisition
Pediatric Cancer Cellular Therapy (CCT) Research Nurse 2 (Hybrid)

The Stanford Cancer Institute (SCI) is one of an elite number of National Cancer Institute‑Designated Comprehensive Cancer Centers in the country, and is a prominent, dynamic, growing and complex Institute within the Stanford University School of Medicine. The SCI actively works to build synergies and collaborations among faculty with cancer‑relevant expertise from four Schools and over 30 departments across Stanford University.

We seek a Research Nurse 2 to help us enact our mission to reduce cancer mortality through comprehensive programs of cancer research, treatment, education and outreach. Given the SCI’s mission, breadth, and depth, it employs over 320 staff members in a fast‑paced, team‑oriented, and forward‑thinking environment with tremendous opportunities for personal and professional growth. The Clinical Trials Office (CTO) is an integral component of the Stanford Cancer Institute since the vital work performed there enables our adult and pediatric cancer centers to translate research from the laboratory into the clinical setting.

You will be working with an unparalleled leading‑edge community of faculty and staff who are fundamentally changing the world of health care in the cancer cellular therapy arena.

Reporting to the Pediatric Hematology/Oncology Clinical Research Nurse Manager, the Research Nurse 2 will be conversant in the goals, mission and priorities of the Institute, and utilize this knowledge to safely enroll and maintain follow‑up for children and adults in Pediatric CCT studies. We are seeking candidates with excellent communication, organization, prioritization, multi‑tasking and clinical skills. Our staff run toward challenges, and you will have a demonstrated history of doing the same with a high degree of professionalism, initiative and flexibility.

Responsibilities include understanding and knowledge of currently open studies and acting as a resource for both faculty and clinical research staff.

Duties
  • Ensure the safety of study participants and maintain communication with their families/caregivers and clinicians.
  • Provide clinical and administrative nursing support and oversight for research clinical trials based on scope of practice. Collaborate with clinical staff, researchers, outside vendors, and other staff to administer treatment and study protocols. May coordinate multi‑site studies.
  • Develop and manage budget for research study, and oversee resources including funds, personnel, and equipment as needed. Coordinate and collaborate with principal investigator to review study protocol and assess and analyze feasibility, budget projections, and staffing needs.
  • Conduct study participant evaluations according to the study protocol, assess adverse events, and apply triage and judgment to determine course of action.
  • Oversee and potentially administer medications and treatments per study protocol for out study participant research participants.
  • Comply with institutional policies, standard operating procedures, and guidelines, and prepare and submit documentation as required by the study protocol, study sponsor, and regulatory authorities. Interpret complex protocols and regulatory requirements. Oversee and manage essential regulatory documents and handle confidential information (verbal and written) with tact and diplomacy, adhering to all HIPAA guidelines.
  • Supervise non‑clinical research staff as needed.
  • Identify, recruit, and enroll study participants, as well as maintain study participant records and determine study participant criteria.
  • Host external audits (Food and Drug Administration, National Institutes of Health, etc.).
  • Support sponsor investigator research with Investigational New Drug/Investigational Device Exemption…
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