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Oversee site monitoring and management, ensure compliance with protocols, and facilitate recruitment and training for clinical studies.

The Clinical Research Associate will conduct monitoring visits, ensure compliance with study protocols, manage site communications, and support regulatory submissions and study management.

The Clinical Research Associate will monitor sites for Oncology studies, ensuring compliance with protocols and managing communications and documentation.

The Senior Clinical Research Associate will monitor clinical trial sites, ensure regulatory compliance, assess site performance, and support recruitment and study execution efforts.