Clinical Research Associate, Sponsor Dedicated
IQVIA · Carlsbad, CA +1 more
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Role summary
This role involves conducting site monitoring visits, managing study progress, and ensuring protocol adherence across assigned clinical trials. The position requires tracking enrollment, coordinating training, managing documentation, and collaborating with research sites to maintain compliance with GCP and ICH guidelines. A bachelor's degree in a scientific field and at least one year of on-site monitoring experience are required.
Privacy & handoff
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