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Manager, Regulatory Affairs, Advertising & Promotion

Job in Edison, Middlesex County, New Jersey, 08818, USA
Listing for: BioSpace
Full Time position
Listed on 2026-07-18
Job specializations:
  • Marketing / Advertising / PR
    Marketing Communications, Marketing Manager
Salary/Wage Range or Industry Benchmark: 128600 - 210000 USD Yearly USD 128600.00 210000.00 YEAR
Job Description & How to Apply Below

Build Our Future Together

At Regeneron, we use science and innovation to develop life‑changing medicines for people with serious diseases. We are seeking a Manager to join our Regulatory Affairs Advertising and Promotion team.

In this role, you will apply clinical development knowledge in concert with an experienced understanding of advertising and promotion regulations/guidances to the development of key product messages presented in Biologic License Applications (BLAs) and Marketing Authorization Applications (MAAs). This individual will provide regulatory advertising and promotion expertise to relevant stakeholders, typically carrying out the responsibilities with guidance from the Regulatory Affairs, Advertising and Promotion Director.

The Manager will oversee therapeutic area(s) and ensure that messages are translated into advertising and promotion initiatives that meet the commercial teams’ objectives while maintaining the necessary state of compliance and corporate integrity.

This position offers the opportunity to contribute to a fast‑growing, science‑driven organization making a meaningful difference to patients worldwide.

When & Where
  • Work Location:

    Sleepy Hollow, NY or Warren, NJ
  • Hybrid: 4 days per week on site
Discover Your Role
  • 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 Director.
  • Creatively contribute to advising on the development of product messages and materials across multiple functional areas.
  • Provide timely regulatory advice and guidance 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 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 relationships 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, maintaining effective communication with FDA OPDP reviewers regarding 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 and guide them on the impact of enforcement activities on company policies.
  • Identify process improvement for promotional review activities that enable portfolio‑wide standardization of policies.
  • Cross‑train across products/indications to ensure continuous regulatory A&P support is provided to stakeholders.
  • Collaborate with regulatory therapeutic area leads to review key marketing application summary documents and study reports.
  • Provide input during review cycles to reflect commercialization objectives and messages in submission documents/reports submitted to health authorities.
  • Provide input to management during labeling development and negotiation to reflect commercialization objectives and messages that impact promotion and advertising.
This Role Requires
  • 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; an advanced scientific degree (e.g., Master’s, PharmD, Ph.D) is preferred.
  • Knowledge of regulations, guidelines, and precedents related to pharmaceutical product development and marketing, focusing on advertising and promotion.
  • Experience with pharmaceutical products required; biologics experience is a plus.
  • Experience working…
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