Regulatory Affairs Group Director, Late Cvrm Regulatory Affairs

AstraZeneca

Mississauga, Ontario, Canada
Hybrid
Extensive regulatory affairs experience
Leading major first wave submissions
Line management of 7-12 staff
The role involves leading a group of 7-12 regulatory professionals within the Cardiovascular, Renal and Metabolic Disease Areas

Job Summary

  • The role involves leading a group of 7-12 regulatory professionals within the Cardiovascular, Renal and Metabolic Disease Areas.
  • Candidates must have extensive experience in drug development, preferably including leading major first wave submissions.
  • The position offers a collaborative culture with flexible working arrangements requiring face-to-face office presence three days a week.

Matching Summary

The role involves leading a group of 7-12 regulatory professionals within the Cardiovascular, Renal and Metabolic Disease Areas.

Skills & Requirements

Must-have

  • Extensive regulatory affairs experience
  • Leading major first wave submissions
  • Line management of 7-12 staff
  • Drug development lifecycle knowledge
  • University Degree in Science

Nice-to-have

  • Experience with complex regulatory procedures
  • Strong influencing and negotiating skills
  • Collaborative culture engagement
  • Continuous improvement project drive
  • Face-to-face office collaboration

Key Requirements

  • University Degree in Science or related subject
  • Proven leadership and project management experience
  • Biopharmaceutical industry regulatory experience

Work Rights

Not specified

Tailored Resume

Cover Letter