Hours could be 0-40

All shifts as needed, possibly 12 hour shifts too (primarily weekend or doubles on the weekend. Could ask for 4 hour shifts too for some studies

ICU is preferred, telemetry, or emergency room experience

At least 1year experience

Active Illinois license

• Participate in the execution of protocol activities of a Phase I clinical research study conducted at the Phase 1 Unit.

• Maintain safety and confidentiality of study subjects throughout the study

• Evaluate adverse events and manage safety reporting activities in a timely manner.

• Review protocols and informed consent forms for scheduled studies, identify, and communicate potential issues to the appropriate personnel.

• Participate in nursing study related activities as required by protocol in compliance with corporate, divisional, and depart-mental SOP’s and external (CFR, ICH, GCP) regulatory guidelines.

• Communicate with the Principal Investigator and other study physicians, Recruiting/Screening, Data Systems, and other personnel to organize study-specific nursing activities.

• Participate in quality and compliance improvement initiatives and provide feedback as appropriate.

• Maintain accurate and complete source data in eSource and/or other source documents and facilitate the resolution of source discrepancies or issues, as appropriate.

• Facilitate training of new nursing personnel and ensure management is apprised of trainee progress.

• Participate independently in the recruitment and screening activities to ensure appropriate enrollment of subjects into studies scheduled at the Phase 1 Unit. *

• Must have nursing skills (Start IVs, computer, dressings, assessment skills to name a few)

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