Director, US Regulatory Advertising and Promotion

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Field of work:
Regulatory & Medical

Posting Date: 30 Jan 2026

Your Role:

The US Regulatory Advertising and Promotion Director oversees and guides the development of advertising and promotional materials, ensuring they meet U.S. regulatory standards while supporting clear, truthful, and compliant communication that aligns with corporate and brand objectives.

This is a hybrid role
, based out of LEO’s Madison, NJ office.

Your Responsibilities:

Act as a key regulatory affairs expert within the LMR team, providing expertise on regulatory strategy, process, filing, best practices, etc. in conjunction with leadership.

Provide strategic and operational leadership for promotional, educational, and investigative communications

Review and evaluate materials submitted by teams to ensure that the content, quality, and format comply with applicable laws, regulations, and client policy.

Uses extensive knowledge of US regulatory requirements and the ability to apply knowledge both strategically and operationally to development projects and marketed product regulatory issues to support clients' corporate goals.

Maintain knowledge of changing regulatory requirements and advise teams as appropriate.

Represent the regulatory affairs team in other meetings or work streams (labeling); provide support for ancillary projects.

Interpret and apply FDA guidance