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Responsible for monitoring study sites, managing site-related activities, and ensuring compliance with regulations and project plans.

Manage clinical study sites, ensuring adherence to protocols and regulations. Conduct monitoring visits and maintain regulatory documents. Prepare reports and train new employees.

The Site Navigator II coordinates site activities during clinical study phases, ensuring compliance, effective site management, and collaboration among stakeholders.

The Clinical Research Associate II is responsible for site monitoring, management of study files, conducting visits, liaison with vendors, and ensuring compliance with regulatory requirements.