Associate Director/director – Risk Management Scientist Global Patient Safety

Eli Lilly UK

Unknown, Unknown, United Kingdom
Base: $115,500 - $169,400; bonus/equity: eligible ...
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Strategic risk minimization guidance
Rmp armm rem development and maintenance
Cross-functional team leadership
** Eli Lilly UK is seeking an Associate Director/Director in Risk Management within Global Patient Safety to provide strategic guidance on risk minimization strategies for pharmaceutical products. The role requires a blend of scientific knowledge and regulatory expertise, as well as strong collaboration and communication skills to influence product teams and manage risk across the product lifecycle. **

Job Summary

  • The role involves providing strategic guidance to cross-functional teams on optimal risk minimization strategies for assigned products.
  • Candidates will lead regulatory interactions including health authority meetings and responses to regulatory questions regarding risk management.
  • Lilly offers a comprehensive benefit program including medical, dental, vision, prescription drug benefits, and a company-sponsored 401(k).

Matching Summary

Match Score: 75

** Eli Lilly UK is seeking an Associate Director/Director in Risk Management within Global Patient Safety to provide strategic guidance on risk minimization strategies for pharmaceutical products. The role requires a blend of scientific knowledge and regulatory expertise, as well as strong collaboration and communication skills to influence product teams and manage risk across the product lifecycle. **

Salary

Base: $115,500 - $169,400; Bonus/Equity: Eligible for company bonus; Benefits: Comprehensive program including 401(k) and medical

Skills & Requirements

Must-have

  • Strategic risk minimization guidance
  • RMP ARMM REM development and maintenance
  • Cross-functional team leadership
  • Regulatory interaction management
  • Benefit-risk assessment frameworks

Nice-to-have

  • Mentoring junior team members
  • Championing organizational optimization
  • External working group representation
  • EU QPPV role support
  • Observational study collaboration

Key Requirements

  • Bachelor's degree in scientific or healthcare field
  • 5 years experience in Clinical Development
  • 2 years experience in patient safety
  • Advanced degree strongly preferred with 3+ years clinical development experience

Work Rights

Not specified

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