CA$171,000 – CA$189,000
Listed on Moderna’s own careers site. You apply with them directly — we never stand between you and the employer.
What this role is
An experienced regulatory leader will shape mRNA medicine development strategy for Canada, managing Health Canada submissions and serving as the primary agency liaison while mentoring junior staff and championing innovation in regulatory approaches.
Our summary, not Moderna’s wording. The full posting is on their site.
Skills this role names
Log in to see which of these are already on your profile.
What they ask for
Required
- BA/BS in scientific/engineering/healthcare discipline
- 8+ years progressively responsible regulatory affairs experience
- Significant experience leading Canadian regulatory strategy and submissions
- Demonstrated leadership and cross-functional influence capabilities
- In-depth knowledge of Canadian regulations and Health Canada processes
- Ability to interpret F&DA, GCP/GMP, PAAB Code, Health Canada policies and ICH guidelines
- Track record leading major regulatory submissions and Health Canada interactions
- Expertise in CTD and eCTD submission builds including Module 1 documents
- Ability to build and maintain Health Canada relationships
- Strong written and oral communication skills
- Experience developing regulatory strategies incorporating business objectives
- Exceptional organizational skills managing multiple high-impact projects
- Advanced problem-solving with proactive approach to regulatory solutions
Nice to have
- Master's, PharmD, or PhD degree
- Experience in biologics, vaccines, rare or autoimmune diseases
- Experience with Generative AI tools for regulatory work