Senior Pharmacovigilance Lead — Safety Strategy (Hybrid)

Bristol-Myers Squibb Co

Warszawa

Hybrid

PLN 118,000 - 142,000

Full time

14 days+

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Job summary

Bristol Myers Squibb Co in Warsaw, Poland seeks a Senior Pharmacovigilance Associate to drive safety data review, SDRMs, and SMT coordination. You will mentor PV staff, manage complex Book of Work, and ensure compliance across PV operations.

The role requires 3–5 years in health sciences or pharma, strong MS Office skills, and proven project leadership with cross-functional teams. Hybrid work options are available.

Qualifications

  • Bachelor-level degree or higher in life sciences or equivalent.
  • 3–5 years of health science/pharma industry experience.
  • Strong understanding of global drug development and safety control.
  • Experience mentoring others and leading projects.
  • Excellent MS Office skills and cross-functional collaboration.

Responsibilities

  • Synthesize safety data from trials, postmarketing, literature to support SDRMs.
  • Contextualize safety trends with product, population and exposure considerations.
  • Schedule SDRMs and maintain safety data review governance.
  • Maintain Signal Tracker and SMT coordination materials.
  • Set up and manage PV systems (SharePoint, OneSafe) and access controls.
  • Support PV processes, documentation and inspection readiness.
  • Lead process improvements across PV operations.
  • Assist in clinical data gathering, tracking, reporting, and follow-up.
  • Build relationships with SMT members and stakeholders.

Skills

Mentoring
Project management
Communication
Safety knowledge
Microsoft Office
Cross-functional collaboration
Pharmacovigilance

Education

BS/RN/MS/PharmD

Tools

SharePoint
OneSafe

Job description

Bristol Myers Squibb Co in Warsaw, Poland seeks a Senior Pharmacovigilance Associate to drive safety data review, SDRMs, and SMT coordination. You will mentor PV staff, manage complex Book of Work, and ensure compliance across PV operations.

The role requires 3–5 years in health sciences or pharma, strong MS Office skills, and proven project leadership with cross-functional teams. Hybrid work options are available.

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