Executive Director, Regulatory Affairs Liaison

Merck & Co., Inc.

Rahway, NJ, USA
Base: $231,900.00 - $365,000.00; bonus/equity: ann...
Hybrid
12 years drug development experience
Majority in regulatory affairs
Securing original nda/bla approvals
The Executive Director will define and execute global regulatory strategy for assigned ophthalmology programs to minimize time to approval

Job Summary

  • The Executive Director will define and execute global regulatory strategy for assigned ophthalmology programs to minimize time to approval.
  • This role requires a leader who can navigate complex regulatory challenges while representing the company at external initiatives and health authority meetings.
  • Candidates are eligible for an annual bonus, long-term incentives, and a comprehensive benefits package including medical, dental, vision, and 401(k) retirement plans.

Matching Summary

The Executive Director will define and execute global regulatory strategy for assigned ophthalmology programs to minimize time to approval.

Salary

Base: $231,900.00 - $365,000.00; Bonus/Equity: Annual bonus and long-term incentive eligible; Benefits: Medical, dental, vision, 401(k), paid holidays, vacation

Skills & Requirements

Must-have

  • 12 years drug development experience
  • Majority in regulatory affairs
  • Securing original NDA/BLA approvals
  • Ophthalmology and retinal disease expertise
  • Leading high-performing global teams

Nice-to-have

  • Experience with small and large molecules
  • Prior Global Regulatory Lead role
  • Cross-cultural awareness and negotiation
  • Strategic input into due diligence
  • Intellectual curiosity and growth mindset

Key Requirements

  • B.S./M.S. in biological science with 12+ years experience
  • M.D./Ph.D. or PharmD. with 9+ years experience
  • Minimum 7 years in regulatory affairs
  • Demonstrated success in securing NDA/BLA approvals
  • U.S. and international regulatory affairs experience

Work Rights

Not specified

Sponsorship: available

Tailored Resume

Cover Letter