Job Description:
Responsibilities:
- 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 ACPRU's 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)
Skills:
- ICU is preferred, telemetry, or emergency room experience
- At least 1year experience
- Active Illinois license
Job Types: Full-time, Contract
Pay: $30.00 per hour
Expected hours: 40 per week
Benefits:
Medical specialties:
Standard shift:
- Day shift
- Evening shift
- Night shift
Weekly schedule:
Experience:
- Nursing: 5 years (Required)
- ICU: 4 years (Required)
License/Certification:
- Active RN Licence in IL (Required)
Ability to Relocate:
- North Chicago, IL: Relocate before starting work (Required)
Work Location: On the road