Sr Risk Management Scientist, Global Pharmacovigilance

GE HealthCare

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Global pharmacovigilance risk management
Safety signal detection and evaluation
Regulatory compliance in pharmacovigilance
** The Senior Risk Management Scientist at GE HealthCare will provide operational support for global pharmacovigilance risk management, focusing on safety signal detection and regulatory compliance. The role requires significant pharmaceutical experience and an advanced clinical degree, with a strong emphasis on collaboration across various teams. **

Job Summary

  • The Senior Risk Management Scientist provides scientific and operational support for global pharmacovigilance risk management and safety signal activities across the product lifecycle.
  • This position contributes to the development of Risk Management Plans, safety analytics, and governance deliverables, and supports preparation of materials and presentations for the Product Safety Review Board.
  • GE HealthCare offers a culture that fosters care, collaboration, and support with total rewards designed to unlock ambition and provide career opportunities.

Matching Summary

Match Score: 75

** The Senior Risk Management Scientist at GE HealthCare will provide operational support for global pharmacovigilance risk management, focusing on safety signal detection and regulatory compliance. The role requires significant pharmaceutical experience and an advanced clinical degree, with a strong emphasis on collaboration across various teams. **

Skills & Requirements

Must-have

  • global pharmacovigilance risk management
  • safety signal detection and evaluation
  • regulatory compliance in pharmacovigilance
  • development of Risk Management Plans
  • cross-functional collaboration
  • safety analytics and data visualization
  • project management skills

Nice-to-have

  • strong oral and written communication skills
  • leadership and interpersonal skills
  • scientific and analytical thinking
  • ability to lead programs and projects
  • inclusion and diversity focus

Key Requirements

  • Advanced clinical degree (MD, DO, NP, PA, PharmD, PhD)
  • Significant pharmaceutical/biotechnology PV experience
  • Experience with clinical trial and post-marketing safety
  • Strong knowledge of FDA, EU, ICH pharmacovigilance guidelines
  • Global pharmacovigilance experience preferred

Work Rights

Not specified

Tailored Resume

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