Associate Director, Global Regulatory Advertising and Promotion

Responsibilities

• Ensuring compliance with regulatory requirements for promotional and non‑promotional materials
• Leading discussions for assigned products during the Promotional Material Review Team (PMRT)
• Supporting interactions with regulatory authorities
• Preparing regulatory submissions for promotional materials
• Developing and delivering training programs on promotional regulations
• Monitoring enforcement actions and industry trends

• Bachelor’s degree in a relevant field (e.g., Life Sciences, Pharmacy, Regulatory Affairs, or a related discipline)
• Minimum 5 years of experience in Regulatory Affairs
• At least 2 years focused on advertising and promotion in the pharmaceutical, biotech, or medical device industry
• Strong knowledge of applicable regulations and enforcement trends
• Prior experience working with cross-functional review committees in a regulated environment
• Familiarity with digital and social media promotional compliance is a plus
• Strong written and verbal communication skills

Demonstrates expertise in Regulatory Affairs with a focus on compliance for promotional materials in the pharmaceutical, biotech, or medical device industries. Proficient in preparing regulatory submissions and leading cross‑functional discussions while ensuring adherence to applicable regulations and industry trends.