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Position Title: Research Nurse II
Work Location: North Chicago, IL 60030, Night shift, including overnight hours and weekend coverage
Assignment Duration: 12 Months
Work Schedule: 12-hour shift: Approximately 7:00 PM-7:00 AM; 8-hour shift: Approximately 11:00 PM-7:00 AM. Variable hours (typically 16-24 hours per week, up to 40 hours based on census, zero hours during census drops/major holidays).
Work Arrangement: Onsite (Remote computer-based onboarding training during daytime hours) Position Summary: The Research Nurse II supports clinical research activities in the Phase I unit, providing nursing care and monitoring research participants during clinical studies. The role requires a nurse who can work independently during night shifts, recognize potential medical concerns, assess participants, and respond appropriately to urgent situations. Key Responsibilities:
* Provide nursing support to clinical research participants in the Phase I unit.
* Monitor participants and assess their condition during overnight hours.
* Recognize changes in participant status and respond appropriately to urgent situations.
* Perform venipuncture when the unit technician is unable to obtain a blood sample.
* Start IVs when required.
* Support evening dosing activities and observe participants according to study requirements.
* Provide post-procedure monitoring when needed, including care following lumbar punctures.
* Complete direct data entry in the facility's clinical research computer system.
* Review study schedules and ensure required activities are completed.
* Complete required computer-based training and follow study and unit procedures.
* Coordinate with other nursing staff and work independently during assigned shifts. Qualification & Experience:
* Active Illinois nursing license. * Strong clinical assessment and judgment skills.
* Ability to recognize and respond to urgent medical situations.
* Ability to work independently during overnight shifts.
* Availability for night-shift coverage and flexibility to accept scheduled shifts.
* Comfort with participant monitoring, clinical documentation, and nursing responsibilities in a research setting.
* Preferred Clinical Backgrounds: Emergency Room (ER), Intensive Care Unit (ICU), Telemetry, Medical-Surgical (Med-Surg). Any one of these backgrounds can be suitable.
* At least one year of nursing experience is the preferred benchmark.
* Clinical research nursing experience (preferred/trainable).
* Experience with adverse-event documentation and safety reporting (preferred/trainable).
* Familiarity with informed consent procedures (preferred/trainable).
* Experience with IV initiation, venipuncture, and participant monitoring. * Experience using electronic clinical documentation systems, such as Epic or similar platforms.
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