Summary The Central Monitor (CM) plays a key role for Data Surveillance by overseeing and supporting clinical trials through centralized monitoring activities. This role ensures data quality, identifies potential risks, and enhances trial oversight by leveraging data analytics and risk-based monitoring strategies. The CM collaborates with cross-functional teams to ensure compliance with study protocols, regulatory requirements, and Valuable Clinical Practice (GCP) guidelines. The
📌 Central Monitor (Data Surveillance Lead) (Hyderabad)
🏢 Novartis España
📍 Hyderabad
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