Director, US Regulatory Advertising & Promotion

Leo Pharma; Madison (NJ); On-site; USD 215,000 - 250,000; Full time

Job summary

LEO Pharma in Madison, NJ is seeking a Director, US Regulatory Advertising and Promotion to lead the regulatory strategy for promotional materials and ensure compliance with FDA standards. This hybrid role is based at LEO's Madison, NJ office and emphasizes leadership within the LMR team.

You will oversee regulatory strategy, review content for regulatory and policy compliance, and collaborate across functions to support corporate objectives.

Qualifications

• 8-10+ years pharmaceutical regulatory affairs experience within Advertising and Promotion.
• Bachelor's degree; advanced degree in a science discipline preferred.
• Broad experience across multiple therapeutic areas.
• Must have Veeva experience.
• Ability to work independently and to be innovative in tackling operational challenges.
• Team-oriented, adaptable, and effective in fast-paced environments.
• Self-motivated, responsible, and high-energy professional.

Responsibilities

• Act as a regulatory affairs expert within the LMR team, guiding regulatory strategy and process.
• Provide strategic and operational leadership for promotional, educational, and investigative communications.
• Review materials to ensure content complies with laws, regulations and client policy.
• Apply FDA guidance and regulatory requirements to development projects and marketed product issues.
• Maintain knowledge of changing regulatory requirements and advise teams.
• Represent the regulatory affairs team in labeling and other meetings/workstreams.
• Interpret applicable FDA guidance documents and standards.

Skills

Regulatory affairs experience

Leadership

Independent work

Team collaboration

Education

Bachelor's degree in science

Advanced degree preferred

Tools

Veeva

Job description

Application deadline: Location: Madison 07940, New Jersey, United States
Contract type: Permanent
Job ID: 4767

Role Description

Are you a leader who thrives at the intersection of compliance, strategy, and innovation? Join LEO Pharma and help shape impactful promotional communications that meet FDA standards while advancing business goals.

Your Role:

The Director, US Reguatory Advertising and Promotion 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 workstreams (labeling); provide support for ancillary projects.
• Interpret and apply FDA guidance documents, standards, and relevant laws.

Your Qualifications:

• 8 - 10+ years pharmaceutical regulatory affairs experience within Advertising and Promotion.
• Bachelor's degree, advanced degree in a science discipline preferred.
• Broad experience across multiple therapeutic areas.
• Must have Veeva experience.
• Ability to work independently and to be innovative in tackling operational challenges.
• Team-oriented, adaptable, and effective in fast-paced, high-pressure environments.
• Self-motivated, responsible, and high-energy professional
• Must be able to perform all essential functions of the position, with or without reasonable accommodation.

Your New Team:

As a member of the LMR for Spevigo, you will be interacting with all functions and business owners.

Compensation:

The base salary range for this position is $215,000 -250,000 per year. The base salary range represents the anticipated low and high of the LEO Pharma range for this position. Salary will vary based on various factors such as the candidate's qualifications, skills, competencies, and proficiency for the role. In addition, some positions may include eligibility to earn commissions/bonus based on company and / or individual performance.

Let's pioneer together!

At LEO Pharma, we help people with skin diseases live fulfilling lives by advancing dermatology beyond the skin. We drive dermatology with our knowledge, collaboration, and curiosity, and we are at the forefront of science in developing new medicines. For us, pioneering together is about constantly improving and extending what's possible for each other, our company, and our patients.

We welcome and consider applications from all qualified candidates because we believe that our different perspectives, backgrounds, and attitudes are what enable us to make the best decisions for LEO Pharma and meet the needs of the wonderfully diverse marketplace we operate in.

For certain positions, LEO Pharma might complete a background check conducted by a third party.

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