Note: The job is a remote job and is open to candidates in USA. KPG99 INC is seeking a highly experienced Executive Director or Director of Regulatory Affairs – Advertising & Promotion to support promotional review activities in the addiction treatment space. This role involves serving as a key regulatory reviewer within the MLR review process and ensuring compliance with FDA promotional regulations and current labeling.
Responsibilities
• Serve as the primary Regulatory Ad/Promo reviewer within the MLR review process
• Review and approve promotional materials within Veeva PromoMats
• Ensure consistency with FDA-approved labeling and applicable FDA guidance
• Provide expert interpretation of FDA regulations and OPDP expectations
• Support Form 2253 submissions to OPDP (preferred)
• Review corporate communications and external-facing materials
• Partner closely with Legal and Medical teams to ensure compliant messaging
• Act as an SME on evolving FDA promotional guidance and labeling updates
• Escalate regulatory risks appropriately and professionally
Skills
• 10+ years of hands-on Regulatory Ad/Promo experience within the pharmaceutical industry
• Deep knowledge of OPDP requirements and FDA advertising regulations
• Extensive experience in MLR/PRC review environments
• Advanced proficiency with Veeva PromoMats
• Strong working knowledge of CDER promotional regulations
• Executive presence with the ability to collaborate cross-functionally
• Strong written and verbal communication skills
• Experience submitting Form 2253 materials
• Experience in CNS, behavioral health, or addiction therapeutic areas
Company Overview
• Our business consulting services are led by significant domain depth built on a robust technology-driven services platform. It was founded in 2013, and is headquartered in Hampton, New Jersey, USA, with a workforce of 51-200 employees. Its website is https://www.kpg99.com/.