Clinical Research Nurse II Position

5 days ago

New York, New York, United States NYU Grossman School of Medicine Full time
Job Summary

We are seeking a highly skilled Clinical Research Nurse II to join our team at NYU Grossman School of Medicine. 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
  • Collaborate with healthcare colleagues across all units and departments to support the safe, high-quality, and compliant conduct of oncology clinical research.
  • Conduct thorough research screening visits for potential trial participants, including review of systems, baseline and ongoing AE assessment, and collection of concomitant medications.
  • Collaborate with investigators and study team members to recruit, enroll, and retain patients on clinical trials, ensuring patient safety and protocol fidelity.
  • Prepare for and oversee the safe conduct of study treatment visits per protocol.
  • Provide patients with a thorough explanation of the trial prior to obtaining informed consent and ongoing education throughout the patient's course on trial.
  • Responsible for good quality source documentation related to research visits, adverse events, and concomitant medications in compliance with CTO policies and standard operating procedures.
  • Support and document the informed consent process with non-English speaking individuals per institutional and external regulatory bodies policies and procedures.
  • Collaborate with the CRC(s) in establishing the feasibility of protocol implementation based on knowledge of institutional capabilities and limitations.
  • Develop and conduct outpatient and inpatient infusion nursing in-services for all approved protocols within the DMG.
  • Support the safe conduct of elective inpatient admissions for applicable clinical trials in collaboration with the study team and management.
  • Provide cross-coverage for other DMGs as needed.
  • Respond promptly to queries requiring clinical input or changes to research nurse-generated electronic documentation.
  • Provide timely follow-up to all clinical patient inquiries/concerns.
  • Maintain fluency in disease-specific terminology and broad understanding of disease(s).
  • Provide clinical education to patients on an ongoing basis, including understanding the disease process, protocol-specified treatment, potential side effects, and ongoing informed consent process.
  • 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.
  • Oversee the clinical coordination of patient schedules ensuring overall adherence to protocol-defined criteria.
  • Provide guidance, training, and education to Associate CRCs, CRCs, and Sr. CRCs.
  • Ensure serious adverse events and other reportable information are reported as per regulatory requirements and protocol, institutional, and regulatory timeframes.
Requirements
  • Bachelor's degree in Nursing (BSN) from an accredited institution.
  • New York RN licensure.
  • BLS certification.
  • Maintenance of chemotherapy/immunotherapy certification through ONS.
  • Minimum of 2+ years nursing experience in oncology research nursing or oncology nursing.
  • Computer literacy, including word processing, spreadsheet, and database management skills.
  • Excellent analytical, interpersonal, writing, and verbal communication skills.
  • Ability to manage priorities and deadlines and maintain service level expectations for tasks.
  • Adaptability, independently completes tasks, and works within deadlines and collaborates effectively as part of a team.
  • Commitment to team problem-solving approach using a research and patient-focused model.
  • Ability to multi-task and prioritize in a fast-paced work environment.
  • Organizational skills to function independently and as a member of a professional team.
  • Ability to work with diverse groups of people.
Preferred Qualifications
  • OCN certification.
  • CCRP, CCRC, and/or CRN-BC certifications.
  • Experience with EPIC electronic health record.

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