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IQVIA
Overview
Perform site monitoring and management to ensure study protocols, regulatory requirements, and GCP/ICH guidelines are strictly followed. Manage study progress by tracking regulatory submissions, recruitment, data integrity, and site documentation.
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Compensation
$71,900 - $169,300 / YEAR
Posted
9 days ago
Perform site monitoring and management to ensure study compliance with protocols, regulations, and sponsor requirements. Manage study progress, including regulatory submissions, recruitment tracking, and data integrity verification.
$64,000 - $189,000 / YEAR
1 month ago
The Clinical Research Associate performs site monitoring visits to ensure study protocols, regulations, and sponsor requirements are strictly followed. They manage site progress, including recruitment, data integrity, and regulatory documentation to ensure high-quality study execution.
$71,900 - $189,000 / YEAR
