Clinical Research Nurse II Oncology

1 month ago


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

We are seeking a highly skilled Clinical Research Nurse II to join our team at NYU Langone Health. As a key member of our clinical trials team, you will be responsible for ensuring the safe and high-quality conduct of oncology clinical research, 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 ensure seamless patient care.
  • Conduct thorough research screening visits for potential trial participants, including review of systems, baseline and ongoing AE assessment, and collection of concomitant medications.
  • Recruit, enroll, and retain patients on clinical trials while ensuring patient safety and protocol fidelity.
  • Evaluate patient eligibility for specific studies and prepare for and oversee the safe conduct of study treatment visits.
  • Provide patients with thorough explanations of trials and obtain informed consent, while also providing ongoing education and support throughout the patient's course on trial.
  • Ensure 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, as per institutional and external regulatory bodies' policies and procedures.
  • Collaborate with CRCs to establish feasibility and identify potential barriers to protocol implementation.
  • 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, treating investigator, and/or PI 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, referrals, and medication management as needed.
  • Maintain fluency in disease-specific terminology and standard of care treatment modalities, keeping up to date with changes to standard of care treatment modalities for specific diseases within each DMG.
  • Provide clinical education to patients on an ongoing basis, including understanding the disease process, protocol-specified treatment, potential side effects, and side effects management.
  • 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.
  • Maintain knowledge of current SOC and protocol-specific side effect management guidelines, including chemotherapy/immunotherapy guidelines and infusion reaction guidelines.
  • Perform medication review, education, and reconciliation, as well as investigational medication handling, verification of drug, doses taken, diary review, reconciling discrepancies, education/re-education, and proper return of unused drug.
  • Demonstrate regular attendance and maintain a record of attends for unit-based and department staff meetings and educational sessions.
  • Achieve and maintain the requirements of the oncology clinical research nurse ladder, demonstrating ongoing professional growth.
  • Serve as a preceptor for the Oncology CRN I.
  • Perform chart audits and support audit preparation as needed.
  • Actively engage in safety initiatives to improve processes and workflows.
  • Perform other duties as assigned.
Requirements
  • RN/BSN degree and New York RN licensure.
  • BLS certification.
  • 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, both to function independently and as a member of a professional team.
  • Ability to work with diverse groups of people.

NYU Langone Health is an equal opportunity and affirmative action employer committed to diversity and inclusion in all aspects of recruiting and employment. All qualified individuals are encouraged to apply and will receive consideration without regard to race, color, gender, gender identity or expression, sex, sexual orientation, transgender status, gender dysphoria, national origin, age, religion, disability, military and veteran status, marital or parental status, citizenship status, genetic information, or any other factor which cannot lawfully be used as a basis for an employment decision.



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