Pharmacoepidemiologist

AstraZeneca

Mississauga, Canada
Base: $109,148.80 - $143,257.80; bonus/equity: ann...
Hybrid
Advanced epidemiological theory and techniques
Conduct targeted and systematic literature reviews
Critical appraisal of study designs
The Safety Epidemiology team plans and executes post-authorization safety studies for nearly 100 marketed or pipeline products

Job Summary

  • The Safety Epidemiology team plans and executes post-authorization safety studies for nearly 100 marketed or pipeline products.
  • Responsibilities include designing, executing, analyzing, and reporting studies under high scientific standards and performing rapid data analytics on global electronic healthcare data.
  • AstraZeneca offers a collaborative culture, individualized flexibility with hybrid work, and a commitment to sustainability and public health.

Matching Summary

The Safety Epidemiology team plans and executes post-authorization safety studies for nearly 100 marketed or pipeline products.

Salary

Base: $109,148.80 - $143,257.80; Bonus/Equity: Annual Variable Pay Bonus/Short Term Incentive opportunity and potential long-term incentive program; Benefits: Competitive Flex Benefits & Retirement Savings Program, 4 weeks' paid vacation, annual Personal Days

Skills & Requirements

Must-have

  • Advanced epidemiological theory and techniques
  • Conduct targeted and systematic literature reviews
  • Critical appraisal of study designs
  • Work effectively with collaborators and CROs
  • Substantial hands-on research experience

Nice-to-have

  • Passion for drug safety
  • Collaborative and innovative culture
  • Interest in public health
  • Sustainability focused company

Key Requirements

  • PhD in pharmacoepidemiology, epidemiology or related health science field
  • Interest in pharmacoepidemiology and drug safety career
  • PhD dissertation focus on medicines
  • Experience with secondary/primary data collection studies
  • Knowledge of patient safety databases for RWE
  • Understanding of drug safety and medical terminology
  • Drug safety experience in clinical or post-marketing
  • Knowledge of drug development and life cycle management
  • Experience with international drug safety reporting/regulations

Work Rights

Not specified

Tailored Resume

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