Associate Director, Regulatory Affairs (Global Regulatory Advertising and Promotion)
About The Position
The Associate Director of Regulatory Affairs, Advertising and Promotion (Ad Promo) is a strategic role that partners cross-functionally with Marketing, Medical, Legal, Market Access, Corporate Communications, and other stakeholders to help ensure materials are compliant with country and local regulations, industry standards, and company policies while supporting business objectives. The ideal candidate is a collaborative and solutions-oriented regulatory professional with strong communication and organizational skills and the ability to balance regulatory risk with commercial innovation. The candidate should have experience leading or facilitating US promotional review committees (MLR) and oversight of vendors providing promotional material review (PMR) services in other countries. Experience supporting product launches is preferred.
Requirements
- Bachelor’s degree required; degree in life sciences, pharmacy, regulatory affairs, or related scientific discipline preferred.
- 7+ years of experience in Regulatory Affairs Advertising & Promotion within the pharmaceutical or biotechnology industry.
- Direct Experience leading or reviewing US prescription drug promotional materials required.
- Strong working knowledge of FDA-OPDP regulations and guidance governing pharmaceutical advertising and promotion, enforcement trends, and MLR processes and procedures
- Working knowledge of PMR requirements in other countries
- Familiarity with Veeva PromoMats or similar review systems
Nice To Haves
- Product launch experience
- Experience supporting specialty, rare disease, oncology, or other complex therapeutic areas
- Global promotional regulatory experience
- Experience working in fast-paced or emerging biotech environments
Responsibilities
- Provide regulatory review and strategic guidance for promotional (branded and disease state) and medical communications for US prescription drug products across multiple channels, including digital, social media, websites, emails, print, speaker programs, video testimonials, scientific congresses, and field communications, among others.
- Participate as a core member of MLR meetings and provide clear, practical, and risk-based regulatory recommendations.
- Confidently advise cross-functional teams on promotional strategy, claims development, fair balance, substantiation requirements, and risk mitigation.
- Manage all submissions to FDA Office of Prescription Drug Promotion (OPDP) and Advertising and Promotion Labeling Branch (APLB), including the timely and accurate FDA 2253 submissions of US promotional materials.
- Support review and approval of corporate and external communications, as applicable.
- Monitor and interpret evolving FDA enforcement trends, OPDP untitled/warning letters, and relevant industry developments to proactively advise internal stakeholders.
- Support launch readiness activities
- Contribute to the development and continuous improvement of internal policies, SOPs, guidance documents, and review standards.
- Collaborate effectively across functions to support timely and compliant material development and approvals.
- Provide mentorship and guidance to junior regulatory staff or consultants, as applicable.
- Participate in cross-functional initiatives related to process optimization, digital innovation, and operational excellence.
Benefits
- competitive salaries
- excellent benefit package
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What This Job Offers
Job Type
Full-time
Career Level
Mid Level
