Manager, Regulatory Affairs, Advertising & Promotion

Regeneron Pharmaceuticals • Warren, MI

7h • Hybrid

About The Position

Regeneron is seeking a Manager to join its Regulatory Affairs Advertising and Promotion team. This role involves applying clinical development knowledge and expertise in advertising and promotion regulations/guidances to the development of key product messages for Biologic License Applications (BLAs) and Marketing Authorization Applications (MAAs). The Manager will provide regulatory advertising and promotion expertise to stakeholders, typically with guidance from the Regulatory Affairs, Advertising and Promotion Director. The position oversees therapeutic area(s) to ensure messages align with commercial objectives while maintaining compliance and corporate integrity. This is an opportunity to contribute to a growing, science-driven organization focused on developing life-changing medicines.

Requirements

• A minimum of 2 total years relevant experience, preferably within Regulatory Advertising and Promotion.
• At minimum, a Bachelor's degree (BS) from an accredited college or university in Life Sciences.
• Knowledge of regulations, guidelines and precedents related to pharmaceutical product development and marketing, with focus in the area of advertising and promotion.
• Experience with pharmaceutical products required, biologics experience is a plus.
• Ability to review promotional materials and interact with FDA OPDP/APLB and support launch products/campaigns, while maintaining excellent written/verbal communication skill when giving strategic regulatory advice.

Nice To Haves

• An Advanced Scientific degree (i.e., Masters, PharmD, Ph.D) is preferred.
• Experience working directly/indirectly with the FDA, specifically OPDP/APLB is preferred.
• Ability to support global promotional review, understanding of clinical trial recruitment materials, and familiarity with labeling regulations is desirable.

Responsibilities

• Management of US regulatory activities associated with advertising and promotion of the company’s marketed products.
• Manages commercial activities from a regulatory advertising and promotion perspective with guidance from the Regulatory Affairs, Advertising & Promotion Director.
• Creatively contribute to and advise on the development of product messages and materials across multiple functional areas.
• Provide timely regulatory advice and guidance, with guidance from Regulatory Affairs, Advertising & Promotion Director, to Commercial teams and Medical Affairs with respect to conference exhibit activities, disease awareness and speaker programs.
• Provide review of US and Global (if applicable) product and disease state materials/communications, with guidance from Regulatory Affairs, Advertising & Promotion Director, to support corporate goals and comply with applicable laws, regulations, and guidance.
• Collaborate cross functionally with key stakeholders in areas such as Marketing, Medical Affairs, and Legal.
• Responsible for establishing working relationship and managing communication with regulatory advertising and promotion professionals at co-promote partner companies.
• Help lead and assist in all interactions with the FDA Office of Prescription drug Promotion (OPDP) for assigned company products, responsible for helping to maintain working relationship and effective communication with FDA OPDP reviewers with respect to advertising and promotion matters, including request for advisory submissions.
• Responsible for compliance with promotional material submissions to FDA on Form 2253.
• Monitor the external environment to advise product teams on evolving regulatory requirements related to product and disease state communications.
• Maintain vigilance with respect to FDA promotional enforcement activities; provide stakeholders with updates on a regular basis; in partnership with management, provide guidance to stakeholders with respect to impact of enforcement activities on the company policies.
• Ability to identify process improvement for promotional review activities that would enable the establishment of portfolio wide standardization of policies.
• Ability to cross train across products/indications to ensure continuous Regulatory A&P support is provided to stakeholders.
• Collaboration with Regulatory Therapeutic Area Leads to review key marketing application summary documents and study reports.
• With guidance from management, help provide input during review cycles to reflect commercialization objectives and messages in the submission documents/reports that are submitted to health authorities.
• Provide input to management during labeling development and negotiation to reflect commercialization objectives and messages that impact promotion and advertising.

Benefits

• health and wellness programs (including medical, dental, vision, life, and disability insurance)
• fitness centers
• 401(k) company match
• family support benefits
• equity awards
• annual bonuses
• paid time off
• paid leaves (e.g., military and parental leave)

What This Job Offers

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