Clinical Research Associate: On-Site Monitoring & Compliance
Listed on 2026-10-06
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Healthcare
Clinical Research -
Research/Development
Clinical Research
ICON plc in Chicago is seeking a Clinical Research Associate to serve as the primary liaison between investigational sites and sponsors, conducting site visits and ensuring ICH-GCP compliance. You will manage documentation in CTMS and eTMF, monitor patient safety, and support site staff training while coordinating with CTAs, LTMs, and CTMs.
The ideal candidate has a bachelor’s degree in Life Sciences or is a qualified RN, 2+ years of on-site monitoring experience, and can travel up to 50% across
This is an excellent opening to take on the Clinical Research Associate:
On-Site Monitoring & Compliance role at ICON Strategic Solutions.
The Clinical Research Associate:
On-Site Monitoring & Compliance role at ICON Strategic Solutions is now open for applications in Chicago, IL, United States.
Join us at ICON Strategic Solutions as our next Clinical Research Associate:
On-Site Monitoring & Compliance in Chicago, IL, United States.
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