Associate Director, International Regulatory Affairs Advertising & Promotion

Responsibilities:
- Design and deliver optimized global regulatory strategies, plans, and dossiers aligned with business strategy for marketed and development compounds.
- Implement regulatory advertising and promotion strategies; lead international (ex-US) regulatory strategy for assigned therapeutic areas.
- Review global regulatory/legal/political environment and plan regulatory communications; lead risk management strategies/plans for global regulatory advertising and promotion.
- Provide global regulatory expertise/position for advertising and promotion; maintain knowledge of applicable codes, regulations, and guidance.
- Implement and update policies/procedures supporting global core messaging; support compliance and improvement plans.
- Provide regulatory analysis/interpretations for high-visibility pharmaceutical news; support training/mentorship and resolve decisions with Marketing and Legal.
- Collaborate cross-functionally; manage/lead cross-functional multidisciplinary teams; ensure compliance with international codes and relevant regulations.
- Hybrid role: 3 days in office from AbbVie Mettawa, IL headquarters.

Qualifications:
- Bachelor’s (or equivalent) in a science field: biology, chemistry, microbiology, immunology, medical technology, pharmacy, or pharmacology (required). Master’s/Ph.D./Pharm.D preferred.
- Associate Director: 8+ years pharmaceutical experience with a Bachelor’s; 5+ years with a Pharm.D plus relevant ad promo experience.
- Solid understanding of regulatory advertising and promotion regulations (direct responsibility required). International experience desired but not required.

Benefits (as stated):
- Paid time off; medical/dental/vision insurance; 401(k) for eligible employees; eligible for short-term incentive programs.