Job Description
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
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.