Director, Regulatory Affairs, Advertising & Promotion (Remote)

Regeneron Pharmaceuticals

8d • $205,000 - $341,600 • Remote

About The Position

Regeneron is seeking a Director, Regulatory Affairs Advertising & Promotion Global to join its Regulatory Affairs team and support its global development and commercial business. The role leads advertising and promotion regulatory strategy, shapes product messaging, and supports compliant commercialization activities in collaboration with Commercial, Medical Affairs, Legal, and Regulatory stakeholders. The position is listed as remote in the United States, with the posting also stating “Remote: 5 days per week on site.”

Requirements

• Master's, PharmD, or PhD; alternatively, a bachelor's degree in Life Sciences from an accredited institution.
• Minimum of 7 years of biotechnology or pharmaceutical industry experience.
• Deep expertise in advertising and promotion regulations, guidance, and development precedents.
• Experience supporting pharmaceutical products.
• Experience working directly with FDA Office of Prescription Drug Promotion (OPDP) and Advertising and Promotional Labeling Branch (APLB).
• Experience reviewing promotional materials and supporting product launches or campaigns.
• Knowledge of commercialization strategy, labeling development, and marketing application content.
• Experience leading teams, influencing cross-functional stakeholders, and working with senior management.
• Strong written and verbal communication skills for providing strategic regulatory guidance.

Nice To Haves

• Biologics experience.
• Experience with global promotional review, clinical trial recruitment materials, and labeling regulations.

Responsibilities

• Lead U.S. and global regulatory activities supporting advertising, promotion, and commercialization initiatives.
• Advise on product messaging and promotional materials across functional areas.
• Provide regulatory guidance for conference exhibits, disease awareness, and speaker programs.
• Review promotional and disease-state communications for compliance with applicable requirements.
• Partner with Marketing, Medical Affairs, Legal, and Regulatory Therapeutic Area Leads.
• Oversee FDA promotional interactions, advisory submissions, and Form 2253 compliance.
• Drive process improvements and portfolio-wide promotional policy standardization.
• Build trusted relationships and influence decisions across complex stakeholder groups.

Benefits

• Competitive and comprehensive total rewards package, which may include annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, medical, dental, vision, life and disability insurance, paid time off, and family support benefits.

What This Job Offers

• Job Type: Full-time
• Career Level: Director