Clinical Research Associate: Site Monitoring Lead
Listed on 2026-10-15
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Research/Development
Clinical Research, Research Assistant/Associate
IQVIA is seeking an on-site Clinical Research Associate to monitor studies and manage site operations in the United States. You will conduct site visits, verify data quality, and ensure adherence to the protocol and regulatory requirements.
You will train sites, track enrollment, and maintain essential trial documentation. Requires at least 2 years of independent on-site monitoring experience in a CRO or sponsor setting, strong knowledge of GCP/ICH, and excellent communication skills in English.
This role, Clinical Research Associate:
Site Monitoring Lead at IQVIA, could be your next move.
Join IQVIA and contribute to our ongoing work.
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This posting is for the Clinical Research Associate:
Site Monitoring Lead role at IQVIA, based in San Jose, CA, United States.
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