About the job

As the Head, Regulatory Affairs, General Medicine and Vaccines Canada on the GRA NA team, you will lead a regulatory team to obtain early approvals and ensure regulatory compliance throughout the product lifecycle for Sanofi’s portfolio of development and marketed prescription products.

Main Responsibilities

1. Lead a team covering a portfolio of development and marketed products (80–90% of time).

   • Regulatory Activities and Resources (60% of time): Provide leadership, support submission teams for Health Canada, maintain compliance, evaluate business development opportunities, lead clinical trial regulatory activities, participate in cross‑functional leadership teams, and assist in setting strategic direction.

   • Development of Human Capital (20–30% of time): Manage direct reports, set priorities, give coaching, conduct performance reviews, and implement personal development plans.