Job Summary

• The Executive Director, Regulatory Affairs Liaison reports to the Vice President (VP), General Medicine, and is accountable for defining and executing global regulatory strategy for assigned ophthalmology programs.
• The role provides strategic oversight across ophthalmology programs in the General Medicine Therapeutic Area, ensuring regulatory objectives are aligned with development, evidence-generation, and commercialization priorities.
• The successful candidate will be eligible for annual bonus and long-term incentive, if applicable, and offered a comprehensive package of benefits including medical, dental, vision, retirement, paid holidays, vacation, and sick days.

Matching Summary

Salary

$231,900.00 - $365,000.00; Bonus/Equity: Annual bonus and long-term incentive, if applicable; Benefits: Medical, dental, vision healthcare and other insurance benefits (for employee and family), retirement benefits, including 401(k), paid holidays, vacation, and compassionate and sick days.

Skills & Requirements

Key Requirements

• Minimum 12 years drug development experience (majority in regulatory affairs) with B.S./M.S.
• Minimum 9 years drug development experience (at least 7 in regulatory) with M.D./Ph.D. or PharmD.
• Demonstrated success in securing original NDA/BLA approvals
• Extensive experience in U.S. and international regulatory affairs

Work Rights