Clinical Research Nurse II - Oncology

Th e Clinical Research Nurse II (CRN II) reports directly to the Medical Director of the Cancer Clinical Trials Program and the Administrative Director in Hematology and Medical Oncology. This role is primarily responsible for performing clinical and patient-facing tasks for patients enrolled in clinical trials. The CRN II collaborates with providers to identify eligible patients, reviews consent forms, discusses trial requirements, and ensures compliance with study protocols during patient visits. The nurse also provides clinical perspective to regulatory coordinators to facilitate trial activation. As a clinically facing research staff member, the CRN II will spend the majority of time in clinic, following and evaluating approximately 16–24 patients p er week. Key Responsibilities Administrative Assist principal investigators with protocol review and development Collaborate on quality assurance and protocol-specific materials Research R ecruit and register patients for clinical trials Coordinate scheduling of labs, imaging, admissions, and visits Collaborate with coordinators and disease group staff to complete trials Clinical Coordinate study enrollment, treatment, and study requirements Collaborate with care teams including infusion, radiation, and surgical nurses Educate patients and families on protocols, adapting to age and cultural needs Order and monitor specimens and administer medications as necessary Document in charts and communicate findings to investigators and physicians Provide protocol training and serve as a resource to the healthcare team Monitor patient safety and regulatory compli ance Professional Development Ide ntify areas for growth and set professional goals Engage in professional organizations locally and nationally Participate in committees and prepare reports, articles, and presentations Required Qualifications Cu rrent Registered Nurse license Bachelor of Science in Nursing (BSN) preferred; Associate Degree accepted Experience in clinical research and oncology Strong communication, organizational, and patient car e skills Preferred Qualifications Prior experience in cancer clinical trials Familiarity with regulatory compliance and trial ac tivation #J-18808-Ljbffr Compunnel, Inc.