The Regulatory Intelligence Director (RID) for Cardiovascular, Renal and Metabolism (CVRM) is responsible for providing disease area specific Regulatory interpretation and impact analysis of emerging competitive intelligence. You will work closely with other Intelligence groups within AZ (Regulatory Policy, Intelligence and Regional Strategy (PIRS), Clinical Information Science, and Global Insights, Analytics, and Commercial Excellence (GIACE). You will be the central point person within TA Regulatory Affairs group in leading bespoke Regulatory research for RADs including disease and project level Regulatory strategy, due diligence, disease area strategy, initiatives. You will work closely with TA-VP, Executive Regulatory Science Directors, Global Regulatory Leaders (GRLs) and Regulatory Affairs Directors (RADs) to provide the Regulatory Intelligence aspect of disease areas and product-specific Regulatory strategies.
You will liaison with PIRS on Regulatory policy matters, and lead a coordinated response in providing feedback by obtaining input from key experts and stakeholders in the therapeutic area. You will also work closely with International, China, and Japan RADs regarding disease area-specific guidance and regulatory intelligence aspects in each region, contributing to overall Regulatory landscape per disease. Will be responsible for communicating the Regulatory impact and implications of relevant competitive intelligence to stakeholders and senior management within AZ
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