Associate Director, Ps/epidemiology Science And Execution

Bristol Myers Squibb

Warsaw, Poland
Base: zł411,770 - zł498,973; bonus/equity: + incen...
Hybrid (50% onsite)
Epidemiology concepts and observational study designs
Regulatory submission materials (dsurs/pbrers/rmps)
Post-marketing safety studies (pass/pmr) execution
Bristol Myers Squibb is seeking an Associate Director for their PS/Epidemiology Science and Execution team in Warsaw, Poland. The role involves executing high-profile epidemiological projects while ensuring regulatory compliance and scientific integrity, requiring significant experience in the field

Job Summary

  • This role involves executing the strategic vision of the Epidemiologist with scientific integrity while managing high-profile projects simultaneously.
  • The position requires drafting regulatory correspondence, supporting post-marketing safety studies, and evaluating drug safety signals for benefit-risk profiles.
  • Bristol Myers Squibb offers a wide variety of competitive benefits and programs to support employee goals both at work and in personal lives.

Matching Summary

Match Score: 85

Bristol Myers Squibb is seeking an Associate Director for their PS/Epidemiology Science and Execution team in Warsaw, Poland. The role involves executing high-profile epidemiological projects while ensuring regulatory compliance and scientific integrity, requiring significant experience in the field.

Salary

Base: zł411,770 - zł498,973; Bonus/Equity: Additional incentive cash and stock opportunities available; Benefits: Wide variety of competitive benefits and programs provided

Skills & Requirements

Must-have

  • Epidemiology concepts and observational study designs
  • Regulatory submission materials (DSURs/PBRERs/RMPs)
  • Post-marketing safety studies (PASS/PMR) execution
  • Protocol development and writing for epidemiology studies
  • Safety signal evaluation and benefit-risk assessment

Nice-to-have

  • Hands-on experience with AI for business efficiency
  • Ability to program or perform computations
  • Mentoring junior scientists within the team
  • Cross-functional stakeholder communication skills

Key Requirements

  • Minimum of 6 years of relevant experience
  • Scientific/biomedical degree (BS, MPH, PharmD, PhD, MD)
  • Firm understanding of pharma regulations and clinical trial conduct

Work Rights

Not specified

Tailored Resume

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