Clinical Research Nurse II

4 weeks ago


New York, New York, United States NYU Langone Health Full time
Job Summary

We are seeking a highly skilled Clinical Research Nurse II to join our team at NYU Langone Health. The successful candidate will be responsible for prioritizing and advocating for the best interest of patients enrolled on oncology clinical trials, while maintaining the fidelity of the clinical research protocol and compliance with policies, procedures, and regulations.

Key Responsibilities
  1. Collaborate with healthcare colleagues across all units and departments to support the safe, high-quality, and compliant conduct of oncology clinical research.
  2. Conduct thorough research screening visits for potential trial participants, including review of systems, baseline and ongoing AE assessment, and collection of concomitant medications.
  3. Collaborate with investigators and study team members to recruit, enroll, and retain patients on clinical trials, ensuring patient safety and protocol fidelity.
  4. Prepare for and oversee the safe conduct of study treatment visits per protocol.
  5. Provide patients with a thorough explanation of the trial prior to obtaining informed consent and ongoing education throughout the patient's course on trial.
  6. Responsible for good quality source documentation related to research visits, adverse events, and concomitant medications in compliance with CTO policies and standard operating procedures.
  7. Support and document the informed consent process with non-English speaking individuals per institutional and external regulatory bodies policies and procedures.
  8. Collaborate with the CRC(s) in establishing the feasibility of protocol implementation based on knowledge of institutional capabilities and limitations.
  9. Develop and conduct outpatient and inpatient infusion nursing in-services for all approved protocols within the DMG.
  10. Support the safe conduct of elective inpatient admissions for applicable clinical trials in collaboration with the study team, treating investigator, and/or PI and management.
  11. Provide cross-coverage for other DMGs as needed.
  12. Respond promptly to queries requiring clinical input or changes to research nurse-generated electronic documentation.
  13. Provide timely follow-up to all clinical patient inquiries/concerns and provide referral, follow-up, and/or medication management as needed.
  14. Maintain fluency in disease-specific terminology and broad understanding of disease(s) and standard of care treatment modalities.
  15. Provide clinical education to patients on an ongoing basis, including understanding the disease process, protocol-specified treatment, potential side effects, and side effects management.
  16. Review the Beacon Build Template in collaboration with the Physician Investigator for all trial patients enrolled onto clinical trials within the assigned or covering DMG.
  17. Oversee the clinical coordination of patient schedules ensuring overall adherence to protocol-defined criteria.
  18. Provide guidance, training, and education to Associate CRCs, CRCs, and Sr. CRCs.
  19. Ensure Serious Adverse Events and other reportable information is reported as per regulatory requirements and protocol, institutional, and regulatory timeframes.
  20. Maintain knowledge of current SOC and protocol-specific side effect management guidelines.
  21. Perform medication review, education, and reconciliation, including investigational medication handling.
  22. Demonstrate regular attendance and maintain a record of attends for unit-based and department staff meetings and educational sessions.
  23. Achieve and maintain the requirements of the oncology clinical research nurse ladder demonstrating ongoing professional growth.
  24. Serve as a preceptor for the Oncology CRN I.
  25. Perform chart audits and support audit preparation as needed.
  26. Actively engage in safety initiatives to improve processes and workflows.
  27. Additional responsibilities as needed, including actively participating in the development of SOPs, policy changes, education sessions, quality improvement projects, and supporting the administration of investigational product on a case-by-case protocol-specific basis.
Requirements

To qualify, you must have a BSN, New York RN licensure, and BLS. Maintenance of chemotherapy/immunotherapy certification through ONS is required. A minimum of 2+ years of nursing experience in oncology research nursing or oncology nursing with qualifying experience determined at the discretion of the Director, Clinical Operations is also required.

Computer literacy, including word processing, spreadsheet, and database management skills, is essential. Excellent analytical, interpersonal, writing, and verbal communication skills are also required. The ability to manage priorities and deadlines and maintain service-level expectations for tasks is necessary. Adaptability, independently completing tasks, and working within deadlines and collaborating effectively as part of a team are also essential. A commitment to team problem-solving approach using a research and patient-focused model is required. Ability to multi-task and prioritize in a fast-paced work environment, organizational skills, and ability to work with diverse groups of people are also necessary.

Preferred qualifications include OCN certification, CCRP, CCRC, and/or CRN-BC certifications, and experience with EPIC electronic health record.



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