Description
The Regulatory Affairs Manager, Canada will lead regulatory activities for assigned pharmaceutical product portfolios, develop and execute regulatory strategies, prepare Health Canada submissions, manage clinical trial submissions, maintain regulatory SOPs and Drug Establishment Licenses, and coordinate with local and global cross-functional teams. The role requires at least seven years of regulatory affairs experience in drugs and biologics, knowledge of Canadian Food and Drug Regulations, CTD experience, and familiarity with AI tools. It is a hybrid position with an annual base salary of CAD 107,196.80 to 140,695.80.
