Central Monitor
About this role
About the Role ICON is seeking a Central Monitor to ensure the quality and integrity of clinical trial data through centralized monitoring activities. The role involves hands-on use of CluePoints systems, collaborating with sites and study teams to maintain data quality and patient safety. What You'll Do
- Conduct remote review and analysis of clinical trial data to identify trends, anomalies, and potential risks to patient safety and data quality.
- Collaborate with site personnel and clinical teams to address findings from centralized monitoring activities and implement corrective and preventive actions as necessary.
- Utilize advanced data analytics tools and technology platforms to enhance the efficiency and effectiveness of centralized monitoring processes.
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