Drive impactful regulatory activities with AstraZeneca as a Regulatory Affairs Manager in Canada. Collaborate closely to oversee product portfolios and engage in strategic regulatory initiatives.
This managerial role at AstraZeneca involves leading regulatory strategies and coordinating with cross-functional teams. Candidates must have a minimum of five years in Regulatory Affairs within pharmaceuticals, showcasing expertise in Canadian regulations. You will be integral to preparations for regulatory submissions and managing communication with Health Canada.
Key Responsibilities:
• Manage regulatory activities for product portfolios
• Liaise with Global Regulatory Affairs Teams on strategies
• Prepare regulatory submissions to Health Canada
• Communicate regulatory updates to stakeholders
• Oversee clinical trial-related submissions as needed
Requirements:
• Minimum 5 years in Regulatory Affairs
• Deep understanding of Canadian drug regulations
• Experience with CTD format submissions
• Solid project management and communication skills
• Advanced degree in life science or equivalent experience
Utilize your regulatory expertise to contribute to life-changing medicines at AstraZeneca in Canada.
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