Senior Regulatory Affairs Director - Oncology

AstraZeneca

Base: $211,581.60 - $317,372.40; bonus/equity: sho...
Hybrid (3 days in-office per week)
Advanced degree in science related field
Proven leadership of major regulatory approvals
Experience with global health authority interactions
AstraZeneca is seeking a Senior Regulatory Affairs Director for their Oncology division, tasked with leading global regulatory strategies for complex oncology programs. The ideal candidate will have extensive experience in regulatory drug development and leadership in global product approvals

Job Summary

  • The Senior Regulatory Affairs Director serves as the Franchise Global Regulatory Lead developing and implementing global strategy on complex oncology programs.
  • Candidates must demonstrate strategic leadership skills to contribute to effective product development and promote novel regulatory initiatives internally.
  • AstraZeneca offers a competitive salary ranging from $211,581.60 to $317,372.40 along with short-term incentives and equity-based long-term programs.

Matching Summary

Match Score: 85

AstraZeneca is seeking a Senior Regulatory Affairs Director for their Oncology division, tasked with leading global regulatory strategies for complex oncology programs. The ideal candidate will have extensive experience in regulatory drug development and leadership in global product approvals.

Salary

Base: $211,581.60 - $317,372.40; Bonus/Equity: Short-term incentive bonus and equity-based long-term incentive program available; Benefits: Qualified retirement program (401k), paid vacation, holidays, leaves, medical, dental, vision coverage

Skills & Requirements

Must-have

  • Advanced degree in science related field
  • Proven leadership of major regulatory approvals
  • Experience with global health authority interactions
  • Strategic planning for complex oncology programs
  • Knowledge of drug development processes

Nice-to-have

  • Experience with radio-conjugates development
  • FDA advisory committee interaction experience
  • EMA oral explanation hearing experience
  • Due diligence and business alliance background
  • Novel regulatory tool development skills

Key Requirements

  • Advanced degree in science or equivalent experience
  • Previous demonstrated experience of regulatory drug development
  • Successful leadership of at least one major global regulatory approval
  • Solid knowledge of regulatory affairs in early and late development
  • Broad background in pharmaceutical business and multiple RA areas

Work Rights

Not specified

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