Note: Hours could be 20-40.
Need to have night and weekend availability (primarily weekend) or doubles on the weekend 0645-2315.
For orientation must have the ability to dedicate approximately 6 weeks on all 3 shifts for training.
Job Description: - 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 SOPs 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 ACPRUs 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 enrolment of subjects into studies scheduled at the Phase 1 Unit. *
- Must have nursing skills (Start IVs computer dressings assessment skills to name a few).
Requirements: - Bachelors/associates in nursing.
- ICU is preferred telemetry or emergency room experience.
- At least 1year experience.
- Active Illinois license.