Associate Director, Safety Epidemiology

AstraZeneca

Toronto, Ontario, Canada
Base: $138,240.00 to $181,440.00; bonus/equity: an...
Hybrid
Phd in pharmacoepidemiology or related field
Advanced epidemiological methods application
Real-world data analysis expertise
The role involves leading the strategy, design, and execution of complex post-authorisation safety studies using real-world data to support global patient safety

Job Summary

  • The role involves leading the strategy, design, and execution of complex post-authorisation safety studies using real-world data to support global patient safety.
  • Candidates will collaborate across Global Patient Safety, Regulatory Affairs, and Biostatistics to produce high-quality, decision-ready evidence for regulatory decision-making.
  • AstraZeneca offers a collaborative culture with hybrid work options, competitive compensation ranging from $138,240 to $181,440, and opportunities for scientific leadership.

Matching Summary

The role involves leading the strategy, design, and execution of complex post-authorisation safety studies using real-world data to support global patient safety.

Salary

Base: $138,240.00 to $181,440.00; Bonus/Equity: Annual Variable Pay Bonus and Long-Term Incentive Program eligibility; Benefits: Flex Benefits, Retirement Savings, 4 weeks vacation, Personal Days

Skills & Requirements

Must-have

  • PhD in pharmacoepidemiology or related field
  • Advanced epidemiological methods application
  • Real-world data analysis expertise
  • Regulatory science and FDA/EMA engagement
  • End-to-end study design and delivery
  • Systematic literature review execution

Nice-to-have

  • Experience with AI/ML tools in workflows
  • Familiarity with diversity plan strategies
  • Qualitative and quantitative benefit-risk assessment
  • Mentorship of external partners and junior scientists
  • Publication record in safety epidemiology

Key Requirements

  • PhD in pharmacoepidemiology, epidemiology, or health science
  • Substantial hands-on research experience
  • Proven track record in regulatory contexts (PASS, PMCs)
  • Strong written and oral communication skills
  • Independent scientific leadership capability

Work Rights

Not specified

Tailored Resume

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