Join Moderna as an Associate Director to lead regulatory efforts for mRNA medicines in Toronto. This role focuses on cutting-edge 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
Solid organizational and problem-solving skills Shape the future of mRNA therapeutics through leadership and deep regulatory knowledge at Moderna.

📌 Associate Director Of Regulatory Affairs Toronto (Canada)
🏢 Moderna
📍 Canada