Join Regeneron's Regulatory Affairs team as a Senior Manager, focusing on Canadian projects in a hybrid workplace. Lead strategic regulatory efforts and contribute to life-changing medicine development while enhancing patient outcomes.
In this role, you will act as the primary contact for Canadian regulatory authorities and manage key submissions including clinical trials and marketing applications. Your expertise will help develop global regulatory strategies and ensure compliance with local standards, enhancing efficiency in product development phases.
Key Responsibilities:
• Serve as primary contact for Health Canada meetings • Manage clinical trial and marketing application submissions • Develop high-quality regulatory strategies • Represent Regulatory Affairs on cross-functional teams • Ensure compliance with Canadian regulations
Requirements: • Bachelor’s degree in science; advanced degree preferred • 6–8 years of regulatory submission experience • Experience with Health Canada meetings and product launches • Strong problem-solving and communication skills • Bilingual in French and English is an asset
Utilize your regulatory expertise to drive compliance and innovation at Regeneron, ensuring impactful medicine delivery in Canada. #J-18808-Ljbffr