Executive Director, Regulatory Affairs Liaison

Merck Sharp & Dohme Corp

Base: $231,900.00 - $365,000.00; bonus/equity: eli...
Hybrid
Global regulatory strategy
Ophthalmology drug development
Health authority engagement
The Executive Director, Regulatory Affairs Liaison is accountable for defining and executing global regulatory strategy for assigned ophthalmology programs, ensuring alignment with development, evidence-generation, and commercialization priorities

Job Summary

  • The Executive Director, Regulatory Affairs Liaison is accountable for defining and executing global regulatory strategy for assigned ophthalmology programs, ensuring alignment with development, evidence-generation, and commercialization priorities.
  • This role involves leading and developing a team of Global Regulatory Leads, setting standards for regulatory excellence, and serving as an authoritative regulatory expert in ophthalmology drug development.
  • The company offers a comprehensive package of benefits including medical, dental, vision healthcare, retirement benefits, paid holidays, vacation, and compassionate and sick days.

Matching Summary

The Executive Director, Regulatory Affairs Liaison is accountable for defining and executing global regulatory strategy for assigned ophthalmology programs, ensuring alignment with development, evidence-generation, and commercialization priorities.

Salary

Base: $231,900.00 - $365,000.00; Bonus/Equity: Eligible for annual bonus and long-term incentive; Benefits: Comprehensive package including medical, dental, vision, retirement, holidays, vacation, sick days

Skills & Requirements

Must-have

  • Global regulatory strategy
  • Ophthalmology drug development
  • Health authority engagement
  • Lead high-performing teams
  • Regulatory submissions and labeling

Nice-to-have

  • Growth mindset and intellectual curiosity
  • Navigate complex regulatory challenges
  • Cross-functional and cross-geographical collaboration
  • Subject matter expert in ophthalmology

Key Requirements

  • B.S./M.S. with 12+ years drug development experience (majority in regulatory affairs)
  • M.D./Ph.D. or PharmD with 9+ years drug development experience (7+ in regulatory)
  • Demonstrated success in securing original NDA/BLA approvals
  • Experience building and leading high-performing teams

Work Rights

Not specified

Tailored Resume

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