Clinical Research Associate (CRA 2), Sponsor Dedicated
IQVIA · Overland Park, KS +2 more
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Role summary
IQVIA seeks Clinical Research Associates with 1–2 years of onsite monitoring experience for sponsor-dedicated roles across multiple US locations. Responsibilities include conducting site monitoring visits, managing study progress, ensuring protocol compliance, and maintaining regulatory documentation in accordance with GCP and ICH guidelines. A scientific or healthcare degree and proficiency with clinical research regulations are required.
Privacy & handoff
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