Sr. Director - Global Regulatory Lead - Neuroscience/immunology

Eli Lilly

Indianapolis, IN, United States
Base: $169,500 - $248,600; bonus/equity: eligible ...
Global regulatory strategy development
Neuroscience or immunology therapeutic area experience
Us and canada regulatory submission leadership
The role involves developing and implementing innovative global regulatory strategies for products in the neuroscience and immunology therapeutic areas from portfolio entry to end of life cycle

Job Summary

  • The role involves developing and implementing innovative global regulatory strategies for products in the neuroscience and immunology therapeutic areas from portfolio entry to end of life cycle.
  • The Senior Director will lead a global regulatory team including regional scientists, CMC, and device experts while serving as the primary interface with the Global Brand Development team.
  • Eli Lilly offers a comprehensive benefit program including medical, dental, vision, 401(k), pension, and well-being benefits alongside an anticipated wage range of $169,500 to $248,600.

Matching Summary

The role involves developing and implementing innovative global regulatory strategies for products in the neuroscience and immunology therapeutic areas from portfolio entry to end of life cycle.

Salary

Base: $169,500 - $248,600; Bonus/Equity: Eligible for company bonus depending on performance; Benefits: Comprehensive program including 401(k), pension, medical, dental, vision, and wellness benefits

Skills & Requirements

Must-have

  • Global regulatory strategy development
  • Neuroscience or immunology therapeutic area experience
  • US and Canada regulatory submission leadership
  • FDA and Health Canada agency interaction management
  • Cross-functional team leadership and coaching

Nice-to-have

  • Experience in EU, China, and Japan markets
  • Knowledge of evolving regulatory reform initiatives
  • Demonstrated conflict management skills
  • Ability to foster diversity and inclusion
  • Strategic relationship building with external players

Key Requirements

  • Advanced scientific degree (PhD, PharmD) with 8+ years experience OR Bachelor's with 10+ years
  • Direct experience in clinical and CMC regulatory sciences
  • Proven leadership assignments demonstrating bold leadership and effective communication
  • Experience in regulatory submissions in US, EU, China, and Japan

Work Rights

Not specified

Tailored Resume

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