Clinical Research Associate II
ICON · Chicago, IL
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Role summary
This role requires monitoring oncology clinical trials at investigational sites in the Chicago region, with up to 50% travel. Responsibilities include site visits, compliance oversight, safety monitoring, data management, and collaboration with cross-functional teams. Candidates must have 2+ years of on-site monitoring experience, preferably in hematologic or medical oncology, plus a life sciences degree or nursing background.
Privacy & handoff
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