Project Leader Regulatory Affairs - VIE Contract

Project Leader Regulatory Affairs- VIE Contract 

• Location:Canada, Toronto
• Target start date: 01/08/2026

iMove, the Sanofi VIE Program, is available to citizens of the European Economic Area (EU + Norway, Liechtenstein and Iceland) aged between 18 and 28.

PLEASE NOTE that since this program is primarily an international development program, candidates cannot apply to a VIE assignment in their own country of citizenship.

PLEASE NOTE that applications that are only submitted in French cannot be considered by our non-French speaking partners at Sanofi worldwide. Therefore, only applications that are submitted in English will be considered. Please make sure to apply with your personal email address.

About the job

As Project Leader Regulatory AffairsVIE within our Regulatory Affairs team you’ll will support and lead projects assigned to develop your technical knowledge and project management skills. You will be accountable for the attainment of development products and marketed products objectives.

The Regulatory Affairs, Canada department is responsible for initial and lifecycle registration of drugs and vaccines to Health Canada. The department is also responsible for registration of clinical trials.
Join the engine of Sanofi’s mission — where deep immunoscience meets bold, AI-powered research. In R&D, you’ll drive breakthroughs that could turn the impossible into possible for millions.

Ready to get started?

About Sanofi

We’re an R&D-driven, AI-powered biopharma company committed to improving people’s lives and delivering compelling growth. Our deep understanding of the immune system – and innovative pipeline – enables us to invent medicines and vaccines that treat and protect millions of people around the world. Together, we chase the miracles of science to improve people’s lives.

Main responsibilities:

• Provide regulatory strategic input to local and global teams for product in development and marketed products throughout their life-cycle.
• Develop and execute filing and approval strategies.
• Organize and coordinate meetings at Health Canada.
• Assure the quality and timeliness of regulatory submissions in Electronic Common Technical Document (eCTD) format and approvals.
• Ensure maintenance of compliance for marketed products with a focus on product monographs and drug labels.
• Review promotional and non-promotional material to ensure compliance
• Occasionally, travel to Ottawa/Bridgewater offices.

About you

Experience:

• 1-2 years of experience in regulatory affairs would be an advantage.

Soft and technical skills:

• Strategic mindset.
• Good project management and organizational skills.
• Accurate and precise working attitude.
• Strong time management and prioritization skills.
• Ability to work cooperatively with others across (multifunctional and multicultural) the organization to achieve shared objectives.
• Proficiency in Microsoft Office package and databases.

Education:

• Master’s degree in pharmacy or other life science discipline such as Biology, Medicine, Chemistry or a related field.

Languages:

• Fluent in English (written and verbal).

Why choose us?

• Be part of a pioneering biopharma company where patient insights shape drug development.
• Work at the forefront of AI-powered science that accelerates discovery and improves outcomes.
• Collaborate beyond your expertise, sparking new ideas with diverse, multidisciplinary teams.
• Help improve the lives of millions of people globally by making drug development quicker and more effective. 
• Enjoy opportunities to collaborate beyond your area of expertise, working with diverse teams across science, clinical, and digital fields to spark new ideas and drive breakthroughs. 
• Join a workplace where diversity, equity, and inclusion are at the core, with Employee Resource Groups and leadership programs that celebrate every voice.
• Achieve genuine work-life balance in a supportive R&D environment.