Manager, Ps/epidemiology Science And Execution

Bristol Myers Squibb UK

Warsaw, Poland
Base: zł154,275 - zł186,945; bonus/equity: + incen...
Hybrid (50% onsite)
3+ years relevant epidemiology experience
Scientific or biomedical degree required
End-to-end execution of pass/pmr studies
Bristol Myers Squibb is seeking a Manager for PS/Epidemiology Science and Execution in Warsaw, Poland, who will be responsible for executing epidemiology strategies and ensuring compliance with regulatory frameworks. The ideal candidate should have a scientific background and at least three years of relevant experience in epidemiology and clinical trial safety

Job Summary

  • The role involves translating and executing the epidemiology strategy set by Senior Epidemiology leadership to ensure delivery with scientific integrity.
  • Employees will own end-to-end execution of assigned epidemiology workstreams, from protocol development through study conduct and associated regulatory deliverables.
  • Bristol Myers Squibb offers a wide variety of competitive benefits, services, and programs that provide resources to pursue goals both at work and in personal lives.

Matching Summary

Match Score: 85

Bristol Myers Squibb is seeking a Manager for PS/Epidemiology Science and Execution in Warsaw, Poland, who will be responsible for executing epidemiology strategies and ensuring compliance with regulatory frameworks. The ideal candidate should have a scientific background and at least three years of relevant experience in epidemiology and clinical trial safety.

Salary

Base: zł154,275 - zł186,945; Bonus/Equity: Additional incentive cash and stock opportunities available; Benefits: Wide variety of competitive benefits and programs offered

Skills & Requirements

Must-have

  • 3+ years relevant epidemiology experience
  • Scientific or biomedical degree required
  • End-to-end execution of PASS/PMR studies
  • Regulatory compliance and inspection-ready quality
  • Protocol development and review expertise

Nice-to-have

  • Strong analytical and conceptual skills
  • Ability to work within matrix teams
  • Experience with secondary data analyses
  • Continuous improvement initiative leadership
  • Excellent written and oral communication

Key Requirements

  • Minimum 3 years of relevant experience
  • BS, MPH, Master's, RN, PharmD, PhD, or MD degree
  • Knowledge of clinical trial safety principles
  • Understanding of observational/real-world data studies
  • Familiarity with regulatory frameworks for patient safety

Work Rights

Not specified

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