Join Moderna as an Associate Director to lead regulatory efforts for mRNA medicines in Toronto. This role focuses on innovative submissions and strategic oversight within a growing team.

As Associate Director, you will define regulatory strategies, oversee Health Canada submissions, and ensure high-quality execution across multiple projects. Collaboration with global teams and driving regulatory excellence are key components of your role. This position allows you to shape the future of mRNA therapeutics in Canada, impacting patient care nationwide.

Key Responsibilities:
• Lead the preparation and review of regulatory submissions
• Foster collaboration within the Canadian Regulatory Affairs team
• Maintain strategic oversight of submission lifecycles




• Navigate complex discussions with Health Canada
• Conduct proactive regulatory intelligence to guide strategy

Requirements:
• BA/BS in scientific discipline, Master’s or PhD preferred
• At least 8 years' experience in Regulatory Affairs
• Extensive experience with Canadian regulations
• Proven leadership in cross-functional discussions
• Robust organizational and problem-solving skills

Shape the future of mRNA therapeutics through leadership and deep regulatory knowledge at Moderna.
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📌 Associate Director of Regulatory Affairs (Ontario)
🏢 Moderna
📍 Ontario