Found Description
Join ICON as a Senior Clinical Research Associate in Vancouver and act as a bridge between investigational sites and sponsors while ensuring compliance. This role involves extensive on-site monitoring and patient safety oversight.
As a Senior CRA, you will be responsible for conducting site visits across various stages while ensuring adherence to ICH-GCP and Health Canada regulations. With at least three years of monitoring experience across multiple therapeutic areas, you will manage documentation in CTMS and eTMF systems while supporting staff training and recruitment processes.
Key Responsibilities:
• Act as primary contact between sites and sponsors
• Conduct site visits for selection and monitoring
• Ensure compliance with ICH-GCP and local regulations
• Document site progress and elevate issues as needed
• Support patient safety and AE/SAE reporting
Requirements:
• 3+ years of on-site monitoring experience
• Bachelor’s degree in Life Sciences or equi...
As a Senior CRA, you will be responsible for conducting site visits across various stages while ensuring adherence to ICH-GCP and Health Canada regulations. With at least three years of monitoring experience across multiple therapeutic areas, you will manage documentation in CTMS and eTMF systems while supporting staff training and recruitment processes.
Key Responsibilities:
• Act as primary contact between sites and sponsors
• Conduct site visits for selection and monitoring
• Ensure compliance with ICH-GCP and local regulations
• Document site progress and elevate issues as needed
• Support patient safety and AE/SAE reporting
Requirements:
• 3+ years of on-site monitoring experience
• Bachelor’s degree in Life Sciences or equi...
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