Base: $211,854.40 to $317,781.60; bonus/equity: sh...
Hybrid
10+ years relevant regulatory experience
Leading global drug/biologic development
Experience with major health authority interactions
The Senior Director leads the development and execution of global regulatory strategy for complex, high-visibility rare disease programs from early development through approval
Job Summary
The Senior Director leads the development and execution of global regulatory strategy for complex, high-visibility rare disease programs from early development through approval.
This role requires deep collaboration with senior leaders across clinical, commercial, and medical affairs functions to provide strategic regulatory insight.
The position offers a competitive annual base pay ranging from $211,854.40 to $317,781.60 along with eligibility for short-term incentives and equity-based awards.
Matching Summary
The Senior Director leads the development and execution of global regulatory strategy for complex, high-visibility rare disease programs from early development through approval.
Salary
Base: $211,854.40 to $317,781.60; Bonus/Equity: Short-term incentive bonuses and equity-based awards available; Benefits: Qualified retirement programs, paid time off, health, dental, and vision coverage
Skills & Requirements
Must-have
10+ years relevant regulatory experience
Leading global drug/biologic development
Experience with major Health Authority interactions
Proven leadership of cross-functional teams
Successful global approval track record
Nice-to-have
Multi-regional experience US EU Japan
Rare disease or oncology background
Cell and gene therapy expertise
Due diligence and alliance partnership experience
Coaching and mentorship capabilities
Key Requirements
Advanced degree in a science field
10+ years of relevant industry experience
Experience leading at least one global approval
Knowledge of GxPs and regulatory documentation systems