Oncology Research Nursing Professional (RN), South Bay Cancer Center

A Brief Overview: The Oncology Research Nursing Professional (ORNP) is a Registered Nurse (RN) who collaborates with Clinical Research Staff—including Physicians, Clinical Research Associates (CRA), APPs, Clinical Nurses, Pharmacists, and clinic staff—to coordinate care for patients enrolled in cancer center clinical research trials. As the research expert of the multidisciplinary team, the ORNP works independently and is accountable for the accurate conduct of their assigned cancer research protocol portfolio. Responsibilities include educating the team on the protocol, setting up operational workflows, and ensuring adherence to good clinical practices. Location Stanford Health Care Responsibilities Clinical Trial Management : collaborate with investigators to lead study patient screening, eligibility determination, and enrollment assessments; assess and document signs, symptoms, and changes in patient condition per protocol; manage patient/family phone calls and coordinate orders with physicians, NPs, or PAs; collaborate with CRC to place and remove therapeutic clinical trial flags; plan, coordinate, and complete randomization, patient assessments, treatments, and follow‑up care; demonstrate multitasking, prioritization, and attention to detail to avoid protocol deviations. Informed Consent Process : manage the consent process in compliance with institutional, FDA, IRB, sponsor, and other regulations; educate patients regarding the clinical trial; document education and consent; alert the principal investigator of concerns; ensure signed consent is scanned and aligned with institutional and sponsor processes. Protocol Compliance : assist CRCs with internal/external study monitor visits, site visits, and study close‑outs; develop protocol‑specific Beacon order sets in collaboration with pharmacy and investigators; oversee and promote compliance with protocol procedures and processes; coordinate scheduling of follow‑up visits and diagnostic testing; provide education to nursing staff regarding the clinical trial; ensure adherence to GCP, ICH, FDA, and other regulatory agencies. Follow institutional and regulatory guidelines, ensuring adherence to GCP, ICH, FDA, and California Nurse Practice Act; deliver population‑specific care considering age, culture, and social issues; maintain an organized and efficient work environment; participate in a collaborative, positive work environment; demonstrate professional practice that supports appropriate care and positive working relationships; maintain current knowledge of organizational and regulatory standards; design and provide training and guidance to operational teams; assess feasibility and design workflow for research programs; assist investigators in protocol development; analyze and interpret clinical results; present at research meetings; report on activities and outcomes; perform related duties as assigned; manage multiple clinical research tasks simultaneously; interact with senior staff and act as subject matter expert; precept/mentor new research staff and students; communicate vetted clinical research information at all levels. Education Qualifications BSN or higher-level nursing degree required. MSN highly preferred. Master’s in research or healthcare‑related field preferred. Experience Qualifications 5+ years nursing experience required or 3+ years in an oncology research nurse role. 2+ years of experience in oncology. Experience in clinical research, ICU, other intensive care settings, pediatrics, case management, or nurse navigation preferred. Human subjects’ protection and Good Clinical Practices training (can be completed after hire). Required Knowledge, Skills and Abilities Communicate vetted information at all organizational levels and with internal/external vendors. Highly multitask and manage multiple projects simultaneously across platforms. Understand information flow, solve problems under pressure, manage conflict, adapt to quick changes, work with ambiguity. Expertise with Outlook scheduling, web conferencing, telepresence, and other technology. Team environment experience, senior/staff interaction, volatile environment management. Relationship building, stakeholder management, critical thinking. Advanced written, verbal communication and facilitation skills. Reading and comprehending instructions with minimal directions. Resource management knowledge in projects; financial and business acumen. Advanced proficiency in research management information systems, analytics, and metrics. Preferred Knowledge, Skills and Abilities Previous experience as an oncology research RN or related clinical research. Master’s in a research‑related degree. Licenses and Certifications CA‑RN (Registered Nurse). BLS – Basic Life Support. OCN – Oncology Nursing Certification (preferred). CCRP – Certified Clinical Research Professional (preferred). ONS – Chemotherapy/Biotherapy certification (preferred). ACRP – Association of Clinical Research Professionals (preferred). Equal Opportunity Employer Stanford Health Care (SHC) strongly values diversity and is committed to equal opportunity and non‑discrimination in all of its policies and practices. Accordingly, SHC does not discriminate on the basis of race, color, sex, sexual orientation or gender identity and/or expression, religion, age, national or ethnic origin, political beliefs, marital status, medical condition, genetic information, veteran status, or disability. Qualified applicants with criminal convictions will be considered after an individualized assessment of the conviction and the job requirements. Compensation Base Pay Scale: Generally starting at $83.98 – $111.27 per hour. #J-18808-Ljbffr