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Clinical Research Nurse I
2 months ago
We are seeking a highly skilled and experienced Clinical Research Nurse I to join our team at NYU School of Medicine. The successful candidate will be responsible for conducting research screenings, collaborating with healthcare colleagues, and ensuring patient safety and protocol fidelity.
Key Responsibilities- Conduct thorough research screenings 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.
- Prepare for and oversee the safe conduct of study treatment visits per protocol.
- Provide patients with a thorough explanation of a 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.
- Support and document the informed consent process with non-English speaking individuals.
- Collaborate with the CRC(s) in establishing the feasibility of protocol implementation and identifying potential barriers.
- Participate in feasibility meetings and provide explanations regarding clinically-related obstacles and solutions.
- Create, review, and approve protocol tracking forms prior to study activation.
- Develop and independently conduct outpatient and inpatient infusion nursing in-services for approved protocols.
- Support the safe conduct of elective inpatient admissions for applicable clinical trials.
- 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 standard of care treatment modalities.
- Provide clinical education to patients on 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.
- Ensure treatment plan is correctly built into the Beacon Build Template and communicate promptly with the Investigational Pharmacy team.
- 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 is reported as per regulatory requirements and protocol, institutional, and regulatory timeframes.
- Maintain knowledge of current SOC and protocol-specific side effect management guidelines.
- Perform medication review, education, and reconciliation.
- Bachelor's in Nursing
- New York RN Licensure
- BLS
- Maintenance of Chemotherapy/Immunotherapy certification through ONS required within the first year of the role
- Minimum of 1+ 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
- OCN certification
- CCRP, CCRC, and/or CRN-BC certifications
- Experience with EPIC electronic health record
