IQVIA is seeking a Site Monitoring professional 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, robust communication, and proficiency in MS Office and
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📌 Clinical Research Associate: Site Monitoring & Impact (Quebec City)
🏢 IQVIA
📍 Quebec City
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