Executive Director, Regulatory Affairs Liaison

Merck & Co., Inc.

Rahway, NJ, USA
Base: $231,900.00 - $365,000.00; bonus/equity: ann...
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12 years drug development experience
Regulatory affairs expertise
Nda/bla approval delivery
** Merck & Co., Inc. is seeking an Executive Director for Regulatory Affairs Liaison to oversee global regulatory strategy for its ophthalmology programs. The ideal candidate will have extensive regulatory experience, particularly in ophthalmology, and will provide strategic oversight while leading a team of Global Regulatory Leads. **

Job Summary

  • The role involves defining and executing global regulatory strategy for assigned ophthalmology programs to minimize time to approval.
  • Candidates must demonstrate a proven track record of securing original NDA/BLA approvals while leading high-performing teams.
  • The position offers a competitive salary range of $231,900.00 to $365,000.00 with comprehensive benefits including medical, dental, vision, and 401(k) matching.

Matching Summary

Match Score: 75

** Merck & Co., Inc. is seeking an Executive Director for Regulatory Affairs Liaison to oversee global regulatory strategy for its ophthalmology programs. The ideal candidate will have extensive regulatory experience, particularly in ophthalmology, and will provide strategic oversight while leading a team of Global Regulatory Leads. **

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
  • Regulatory affairs expertise
  • NDA/BLA approval delivery
  • Team leadership and management
  • Ophthalmology program oversight

Nice-to-have

  • Retinal disease regulatory experience
  • Small and large molecule development
  • Cross-cultural awareness
  • Strategic negotiation skills
  • Intellectual curiosity

Key Requirements

  • B.S./M.S. in biological science or related discipline
  • Minimum 12 years relevant drug development experience
  • Majority of experience in regulatory affairs
  • M.D./Ph.D. or PharmD. with 9+ years experience (alternative)
  • Experience as Global Regulatory Lead preferred

Work Rights

Not specified

Sponsorship: available

Tailored Resume

Cover Letter