Advance your career at Moderna in Toronto as the Associate Director of Regulatory Affairs, focusing on robust regulatory strategies for mRNA innovations. Ensure compliance and deliver significant patient advantages.

In this role, you will lead the Canadian Regulatory Affairs team, managing a range of submissions and regulatory interactions with Health Canada. You will develop strategies that align with global initiatives while fostering accountability among stakeholders, ensuring compliance, and meeting Canadian business goals.

Key Responsibilities:
• Drive regulatory submissions for Health Canada approvals
• Collaborate on regulatory strategies with cross-functional teams
• Guide development and execution of regulatory paths




• Lead Canadian labelling activities and compliance
• Conduct regulatory monitoring and strategic planning

Requirements:
• At least 8 years in Regulatory Affairs or similar
• Strong leadership and influencing skills
• Comprehensive knowledge of Canadian regulatory landscapes
• Experience with regulatory submissions for therapeutics
• Excellent communication and prioritization abilities

Impact the future of medicine with your expertise at Moderna in Toronto.
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📌 Moderna Regulatory Affairs Associate Director (Ontario)
🏢 Moderna Therapeutics
📍 Ontario