Research Nurse

The Research Nurse in the Clinical Research Center (CRC) at the Einstein-Montefiore ICTR plays a critical role in the implementation of early-phase and translational clinical research studies. Working as part of a multidisciplinary team, the Research Nurse supports Principal Investigators in conducting high-quality, compliant, patient-centered research. Responsibilities span the full lifecycle of study visits, including subject intake, clinical assessments, specimen collection, protocol adherence, documentation, and patient safety monitoring.

• Conduct subject intake and screening in accordance with approved protocols and IRB requirements.
• Schedule and coordinate study-specific CRC visits (including fasting, pharmacokinetic, and infusion procedures).
• Provide direct clinical care to research participants, including:

• • Assess and monitor the subject's health condition, including history-taking and physical assessments (Anthropometrics; Vital signs; ECG; ABI; etc.)

• Efficient and precise collection of blood, urine, and other body fluids according to research protocol requirements
• Medication administration (including investigational drugs) per protocol

• Ensure adherence to study-specific requirements, including timed specimen collection and documentation of adverse events.
• Collaborate with study coordinators, investigators, pharmacists, lab personnel, and other clinical staff to ensure protocol fidelity and data integrity.
• Maintain accurate and timely documentation in the electronic medical record (EMR) and case report forms (CRFs).
• Support training and orientation of new clinical research staff as needed.
• Maintain exam room and research space readiness, including inventory control and infection control practices.
• Participate in unit-based quality assurance and continuous improvement initiatives.
• Perform additional related duties as assigned to support clinical research operations

Scope of Responsibility

The Research Nurse will work under the direction of the CRC Director and in close coordination with the ICTR’s Clinical Research Center staff, investigators, and coordinators. The role requires independence, judgment, and flexibility, particularly in executing complex protocol procedures and responding to participant needs. The position does not have direct supervisory or budgetary responsibilities but may provide training support to junior staff and students.

• Required:
• Current NYS license and registration as a Registered Professional Nurse (RN)
• Minimum of 2 years of clinical nursing experience, preferably in acute care or ambulatory settings
• Excellent phlebotomy skills and intravenous catheter placement
• BLS certification
• Preferred:
• Prior experience in clinical research or familiarity with Good Clinical Practice (GCP)
• ACLS preferred
• Bachelor’s degree in Nursing (BSN) preferred

Skills and Competencies

• Excellent clinical assessment and critical thinking skills
• Ability to multitask and prioritize in a dynamic research environment
• Strong written and verbal communication skills
• High attention to detail and accuracy in documentation
• Familiarity with research protocols, informed consent, and regulatory documentation
• Comfortable working with electronic health records and data capture platforms (e.g., Epic, REDCap)
• Ability to collaborate across disciplines with professionalism and diplomacy
• Commitment to maintaining confidentiality and ensuring patient safety

*Please note the base hourly rate for the role is listed. This rate does not include your experience differential.