Project Leader Regulatory Affairs - Vie Contract

Sanofi

Toronto, Canada
Fluent in english written and verbal
Master's degree in pharmacy or life science
Project management and organizational skills
This role supports the development of technical knowledge and project management skills within Sanofi's Regulatory Affairs team

Job Summary

  • This role supports the development of technical knowledge and project management skills within Sanofi's Regulatory Affairs team.
  • The position is responsible for initial and lifecycle registration of drugs and vaccines to Health Canada, including clinical trial registration.
  • Candidates must be citizens of the European Economic Area aged between 18 and 28 to participate in the iMove VIE Program.

Matching Summary

This role supports the development of technical knowledge and project management skills within Sanofi's Regulatory Affairs team.

Skills & Requirements

Must-have

  • Fluent in English written and verbal
  • Master's degree in pharmacy or life science
  • Project management and organizational skills

Nice-to-have

  • Strategic mindset for regulatory affairs
  • Experience with Health Canada submissions
  • Ability to work in multicultural teams

Key Requirements

  • 1-2 years experience in regulatory affairs (advantage)
  • Citizenship of EEA countries (EU + Norway, Liechtenstein, Iceland)
  • Age between 18 and 28 years old
  • Cannot apply in own country of citizenship

Work Rights

Must have EEA citizenship and be eligible for VIE program

Tailored Resume

Cover Letter