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IQVIA
Overview
The role involves performing monitoring and site management tasks for various clinical protocols, therapeutic areas, and sites, including conducting site visits (selection, initiation, monitoring, and close-out) according to contractual scope and regulatory guidelines. Key duties include managing protocol training, tracking study progress, ensuring data quality and integrity, and maintaining essential study documentation like the TMF and ISF.
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Compensation
CA$102,500 - CA$170,900 / YEAR
Posted
3 months ago