Senior Pharmacovigilance Associate

Bristol Myers Squibb

Warsaw, Poland
Base: zł117.500 - zł142.377; bonus/equity: + incen...
Hybrid (50% onsite)
Signal detection and data review
Safety management team facilitation
Pharmacovigilance process development
Bristol Myers Squibb is seeking a Senior Pharmacovigilance Associate in Warsaw, Poland, to support drug safety through signal detection and safety data review. The role requires collaboration with cross-functional teams and offers a hybrid work model, allowing for up to 50% remote work

Job Summary

  • The Senior Pharmacovigilance Associate will collaborate with cross-functional stakeholders to provide strategic and operational support across therapeutic areas for signal detection, safety data review, safety management teams, and risk management.
  • The Senior Pharmacovigilance Associate will mentor PV Associate I and II and support professional development.
  • Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives.

Matching Summary

Match Score: 85

Bristol Myers Squibb is seeking a Senior Pharmacovigilance Associate in Warsaw, Poland, to support drug safety through signal detection and safety data review. The role requires collaboration with cross-functional teams and offers a hybrid work model, allowing for up to 50% remote work.

Salary

Base: zł117.500 - zł142.377; Bonus/Equity: Additional incentive cash and stock opportunities may be available; Benefits: Competitive benefits, services and programs

Skills & Requirements

Must-have

  • Signal detection and data review
  • Safety management team facilitation
  • Pharmacovigilance process development
  • Cross-functional collaboration
  • Mentoring junior associates

Nice-to-have

  • Transforming patients' lives through science
  • Supportive culture and global participation
  • Balance and flexibility in work environment

Key Requirements

  • BS/RN/MS/PharmD in life sciences or equivalent
  • 3-5 years professional experience in health science
  • 3 years pharmaceutical or industry experience
  • Thorough understanding of global drug development
  • Demonstrated mentoring experience
  • Demonstrated project management experience
  • Strong understanding of medical concepts
  • Strong knowledge of safety activities in drug development
  • Excellent knowledge of Microsoft Office programs

Work Rights

Not specified

Tailored Resume

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