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Research Nurse Specialist

2 months ago

Duarte, California, United States City of Hope Full time
About the Role

City of Hope is seeking a highly skilled Clinical Research Nurse to join our team. As a key member of our research team, you will play a critical role in the coordination and management of clinical trials, ensuring the highest level of patient care and research integrity.

Key Responsibilities
  • Collaborate with investigators to assess patient eligibility for clinical trials and ensure accurate documentation of trial criteria.
  • Assess and prioritize clinical information for patients enrolled in clinical trials, communicating effectively with physicians, nurses, and other healthcare professionals.
  • Document patient signs and symptoms, reactions to treatment, and changes in physical or psychological condition, ensuring complete and accurate documentation to avoid protocol deviations.
  • Manage patient and family phone calls, collaborating with physicians and other healthcare professionals as needed to obtain orders for patient management.
  • Coordinate and communicate all aspects of care as defined by the protocol with physicians and other healthcare professionals.
  • Collaborate with CRCs to ensure therapeutic clinical trial flags are placed on patients during active treatment and removed when patients are removed from clinical trial participation or treatment is complete.
  • Informed Consent Process
    • Ensure the consent process is performed in compliance with institutional, FDA, IRB, clinical trial sponsor, and other applicable regulations.
    • Participate in the education of patients regarding clinical trials, documenting education in the medical record.
    • Alert principal investigators to any concerns raised by patients during the informed consent process.
    • Assure timely scanning of signed consents into the medical record.
  • Protocol Compliance
    • Assist internal or external study monitors in protocol initiation and collaborate in the review of documentation during protocol audits.
    • Develop, in collaboration with the investigational pharmacy and principal investigator, pre-printed standard research orders for therapeutic clinical trials, ensuring orders are reviewed, approved, and posted in Clinical Trials on Line (CTOL).
    • Promote compliance with protocol procedures and processes as outlined in the clinical trial.
    • Collaborate with scheduling staff to ensure future appointments for patients are scheduled correctly and timely, complying with International Air Transport Association and institutional policies for shipping and receiving of biological specimens, experimental agents, and devices.
    • Provide education to nursing staff regarding clinical trials, ensuring protocol treatment plans are followed and medications are administered safely and as outlined in the clinical trial.
    Requirements
    • BSN degree
    • 2 or more years of experience in oncology, clinical research, research, ICU, other intensive care setting, pediatrics, case management, or nurse navigation
    • Human subjects protection training (can be completed after hire)
    Certifications/Licenses
    • Current California RN License
    • American Heart Association BLS Certification