Drive the future of mRNA therapeutics in Canada with Moderna as a Regulatory Affairs Leader. You’ll craft strategies, lead crucial submissions, and engage with Health Canada while working in a vibrant biotech hub.

Moderna is expanding its impact in Toronto, making it a pivotal location for regulatory affairs specialists. In this role, you will take charge of Canadian regulatory strategies, ensuring alignment with global teams. By leading Health Canada submissions, you will play a critical role in advancing cutting-edge mRNA medicines that improve patient outcomes.

Key Responsibilities:



• Foster collaboration among the Canadian Regulatory Affairs team • Develop and influence regulatory strategies with global teams • Lead Health Canada submission processes and reviews • Provide strategic oversight during the submission lifecycle • Serve as primary regulatory liaison with Health Canada

Requirements: • BA/BS in scientific discipline; Master’s or PhD preferred • 8+ years in Regulatory Affairs and Canadian strategy • Proven track record in leading significant submissions • Expertise in navigating complex regulatory pathways • Robust communication and organizational skills

Utilize your regulatory expertise to impact the future of mRNA medicine at Moderna in Toronto. J-18808-Ljbffr

📌 Regulatory Affairs Leader At Moderna Toronto
🏢 BioSpace
📍 Toronto