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Research - Clinical Trials Nurse
Contract: North Chicago, Illinois, US
Salary Range: 50.00 - 56.00 | Per Hour
Job Code: 371534
End Date: 2026-10-08
Days Left: 11 days, 8 hours left
Hi there, This is Siddhi, Talent Expert with Collabera LLC. Hope this message finds you well! We're hiring for Top performers encouraged to apply positions are filling fast! If interested, Let's connect and don't miss out apply today and let's talk about your next big opportunity!
Email: siddhi.kadakia@collabera.com | Phone: (847)-440-1112.
Position Details:
Email: siddhi.kadakia@collabera.com | Phone: (847)-440-1112.
Position Details:
Client Industry: Pharmaceutical/Medical Device/Biotechnology
Job Title: Research Nurse II/Clinical Trials Nurse
Location: North Chicago, Illinois 60030
Duration: 6 months Contract (++ possibility of extension based on performance and business needs)
Shift: Full time (M-F 7:00 am to 3:30). Training will be on the same schedule
Pay Rate: $50.00 to $56.00 Per Hour.
Top 3-5 skills, experience or education required for this position:
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Communication skills
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Customer Service skills
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Multitasking
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Nursing skills / RN license /RN License required
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MS Office and Electronic Medical Record Platforms
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Experience Level = 3-5 Years
Purpose
The Clinical Research Nurse is a specialized research professional working with and under the direction of the clinical Principal Investigator (PI). Assists with the execution of study-related activities of a Phase I clinical research study. Research nurses should primarily be concerned with the protection and care of research subjects. The primary role is to function as a licensed registered nurse engaged in the practice of care/assessments of the healthy volunteers and/or patient. Position includes disseminating information regarding new information for documentation, performance improvement and data source upgrades.
Responsibilities
- 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 compliance with Corporate, divisional, and departmental SOP’s and external (CFR, ICH Good Clinical Practise) regulatory guidelines. Responsible for compliance with applicable Corporate and Divisional Policies and Procedures.
- Evaluate adverse events and manage safety reporting activities in a timely manner.
- Interact with the Principal Investigator and other study physicians, Recruiting/Screening, Data Systems, and other personnel in support of study-specific activities.
- Support quality and compliance improvement initiatives as appropriate.
- Participate in the recruitment and screening activities to ensure successful enrollment of volunteers into studies scheduled at the Phase 1 Unit. Interfaces with research participants to support efforts to determine eligibility and consenting of study participants according to protocol. Review and assess data collected. Serve as a resource person or act as a consultant within area of clinical expertise (R/S).
- Disburses investigational drug and provides teaching regarding administration, as necessary. Develops accurate source materials and ensures compliance from site staff. Ensures all protocol procedures are completed per study requirements (Unit), Other tasks as assigned.
Benefits:
The Company offers the following benefits for this position, subject to applicable eligibility requirements: medical insurance, dental insurance, vision insurance, 401(k) retirement plan, life insurance, long-term disability insurance, short-term disability insurance, paid parking/public transportation, (paid time , paid sick and safe time , hours of paid vacation time, weeks of paid parental leave, paid holidays annually – These all are subject to applicable eligibility).
Job Requirement
- Clinical Research Nurse
- Research Nurse
- Clinical Trials Nurse
- Registered Nurse
- RN
- Clinical Research
- Clinical Trials
- Phase I Studies
- Patient Assessment
- Research Subject Care
- Protocol Compliance
- CFR
- Adverse Events
- Safety Reporting
- Informed Consent
- Patient Screening
- Participant Recruitment
- Enrollment
- Investigational Drug
- Source Documentation
- EMR
- Electronic Medical Records
- MS Office
- Clinical Research Coordinator
Reach Out to a Recruiter
- Recruiter
- Phone
- Siddhi Kadakia
- siddhi.kadakia@collabera.com
Apply Now
Apply Now
