Project Leader Regulatory Affairs - Vie Contract

Sanofi

Toronto, Canada
Regulatory submissions in ectd format
Project management skills
Regulatory strategic input
As Project Leader Regulatory Affairs VIE within our Regulatory Affairs team you’ll will support and lead projects assigned to develop your technical knowledge and project management skills

Job Summary

  • As Project Leader Regulatory Affairs VIE within our Regulatory Affairs team you’ll will support and lead projects assigned to develop your technical knowledge and project management skills.
  • The Regulatory Affairs, Canada department is responsible for initial and lifecycle registration of drugs and vaccines to Health Canada and registration of clinical trials.
  • Join a workplace where diversity, equity, and inclusion are at the core, with Employee Resource Groups and leadership programs that celebrate every voice.

Matching Summary

As Project Leader Regulatory Affairs VIE within our Regulatory Affairs team you’ll will support and lead projects assigned to develop your technical knowledge and project management skills.

Skills & Requirements

Must-have

  • Regulatory submissions in eCTD format
  • Project management skills
  • Regulatory strategic input
  • Compliance maintenance for marketed products
  • Coordination with Health Canada

Nice-to-have

  • Strategic mindset
  • Strong time management
  • Multifunctional collaboration
  • Proficiency in Microsoft Office
  • Accurate and precise working attitude

Key Requirements

  • 1-2 years regulatory affairs experience
  • Master’s degree in pharmacy or life sciences
  • Fluent English written and verbal
  • European Economic Area citizenship aged 18-28
  • Cannot apply to assignment in own country of citizenship

Work Rights

Must be citizen of European Economic Area aged 18-28; cannot apply in own country of citizenship

Tailored Resume

Cover Letter