Research Nurse II
The Fountain Group · Grayslake, IL · 2 wk ago
On-siteOTHR$43–$46/hrContract
About the role
The Fountain Group is currently seeking a Research Nurse II for a prominent client. This position is located in Grayslake, IL and is 100% onsite.
Responsibilities
- Support execution of Phase I clinical research studies under the direction of the Principal Investigator (PI), with primary responsibility for research participant safety and nursing care.
- Review study protocols and informed consent forms, identify potential issues, and ensure study-related activities are performed according to protocol requirements and applicable SOPs.
- Perform nursing assessments and support the recruitment, screening, eligibility determination, and consenting of healthy volunteers and/or patients participating in clinical studies.
- Evaluate and document adverse events and manage safety reporting activities in accordance with study requirements.
- Coordinate with Principal Investigators, study physicians, Recruiting/Screening, Data Systems, and other study personnel to support study-specific activities.
- Review and assess clinical research data collected during study activities and support quality and compliance improvement initiatives.
- Disburse investigational drugs and provide participant teaching regarding drug administration when required by study protocols.
- Develop accurate source materials and ensure study procedures and documentation comply with protocol requirements.
- Ensure completion of required protocol procedures, documentation, and study activities within the Phase I research unit.
- Maintain compliance with CFR, ICH GCP, Corporate/Divisional policies, and departmental SOPs.
Requirements
- Registered Nurse (RN) license required.
- Nursing education/degree from an accredited nursing program.
Qualifications
- Clinical research nursing experience preferred.
Skills
- Registered Nursing (RN)
- Phase I Clinical Research
- Clinical Research Protocol Compliance
- Informed Consent Processes
- Adverse Event Evaluation & Safety Reporting
- Research Participant Screening & Eligibility Assessment
- Investigational Drug Dispensing & Administration Education
- Clinical Research Source Documentation
- CFR & ICH GCP Compliance
- Electronic Medical Record (EMR) Platforms
- Microsoft Office
Preferred Skills
- Clinical research experience in a Phase I research unit
- Experience working with healthy volunteers and/or research patients
- Experience with clinical trial documentation and source materials
- Experience supporting quality and regulatory compliance initiatives
- Experience working directly with Principal Investigators and study physicians
Pay
$43-$46/hour
Schedule
Monday-Friday, 7:00 AM-3:30 PM; training follows the same schedule.