Advance your career as the Director of Regulatory Affairs for mRNA at Moderna in Toronto. Help shape strategies that ensure the successful delivery of life-changing therapies to patients.

In this influential role, you will guide a team dedicated to navigating Canada’s regulatory landscape. By leading submissions to Health Canada and collaborating with global stakeholders, you’ll drive excellence in regulatory practices while fostering sustainable innovation. This is an opportunity to take part in the cutting-edge world of mRNA medicine.

Key Responsibilities:
• Oversee Canadian regulatory strategies and submissions
• Ensure compliance and accountability in the regulatory process
• Drive collaborative efforts with cross-functional teams




• Provide expert regulatory guidance across development phases
• Engage with Health Canada on regulatory matters

Requirements:
• BA/BS in a relevant field; Master’s, PharmD, or PhD is a plus
• 8+ years of related experience in regulatory affairs
• Demonstrated success in leading Canadian regulatory activities
• Solid knowledge of applicable Canadian regulations
• Exceptional communication and leadership abilities

Join Moderna in Toronto and contribute to the future of healthcare through regulatory excellence.
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📌 Director of Regulatory Affairs for mRNA (Ontario)
🏢 BioSpace
📍 Ontario