Clinical Research Associate – Site Monitoring & Study Oversight
Listed on 2026-10-07
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Research/Development
Clinical Research, Research Assistant/Associate
IQVIA is seeking a site-monitoring professional in the United States to ensure studies are conducted according to protocol, GCP, and sponsor requirements. The role encompasses on-site visits, site training, recruitment collaboration, and regulatory tracking.
Responsibilities include monitoring visits, recruitment planning, training, quality issue escalation, TMF/ISF maintenance, and cross-team collaboration to support project execution and site financial management when applicable.
We would love to welcome a new Clinical Research Associate – Site Monitoring & Study Oversight to our organisation in Ontario, CA, United States.
Full responsibilities and requirements are described in the listing above.
Learn more about the Clinical Research Associate – Site Monitoring & Study Oversight role in the description above.
We appreciate your interest in this position.
Join IQVIA and contribute to our ongoing work.
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