IQVIA is seeking a Site Monitoring qualified to ensure study sites conduct and report data per protocol and sponsor requirements. You will monitor visits, support recruitment plans, and manage regulatory submissions while maintaining TMF/ISF documentation.
Communicate with sites and study teams to address issues and keep projects on track. The role requires a science/healthcare degree or equivalent experience, with GCP/ICH knowledge, strong communication, and proficiency in MS Office and
📌 Clinical Research Associate: Site Monitoring (Canada)
🏢 IQVIA
📍 Canada
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