The Ravitz Cancer Center Research Unit (CCRU) is seeking an experienced and detail-oriented Registered nurse to join our dynamic team. This role involves the critical analysis and support of research protocols and ensuring seamless integration into our infusion center operations. The ideal candidate will be committed to advancing cancer research through meticulous protocol review, documentation preparation, education of staff, and direct patient care. This is a multi-faceted position that requires a deep understanding of infusion workflows, SOPs, general nursing practice, guidelines, and policies.
Key Responsibilities:
Review and analyze research protocols for compliance with regulatory standards and identify special requirements for the infusion center.
Prepare concise summary workflow documents outlining infusion center protocol requirements.
Examine draft research prescriptions to ensure they align with the study protocols
Develop and maintain visit-specific workflow documents for the Ravitz CCRU as per protocol stipulations.
Educate infusion research staff regarding the special or unique requirements of study protocols.
Create and adjust research infusion durations to optimize patient care and adherence to protocols.
Monitor queries from the Clinical Trial Support Unit concerning protocol deviations and address them accordingly.
Provide comprehensive support to the Ravitz infusion team, which includes direct patient care responsibilities.
Respond to inquiries from the research pharmacy, assisting with protocol-related questions.
Offer insights into infusion workflows, Standard Operating Procedures (SOPs), and general nursing practices and policies to enhance research operations.
The RN administers investigational agents including but not limited to injections, IV hydration, blood products, chemotherapy, biotherapy and immunotherapy.
Expectations:
Knowledge of clinical research processes, protocol design, and regulatory requirements.
Excellent interpersonal and communication skills for education and coordination with a multidisciplinary team.
Ability to work independently, manage complex projects with attention to detail, and handle sensitive information confidentially as measured by interview, references, and performance evaluations
Proficiency with electronic medical record (EMR) systems
Demonstrated critical thinking skills and problem-solving abilities in a clinical setting.
Commitment to providing the highest level of care and support to patients participating in clinical trials.
Demonstrated ability to start IV?s, access ports and maintain vascular access