Senior Manager, US Regulatory Affairs - Ad & Promo

ABBVIE; Irvine (CA); Hybrid; USD 125,000 - 237,000; Full time

Job summary

AbbVie in Irvine, CA seeks a Senior Manager Regulatory Affairs US Advertising and Promotion to lead regulatory, scientific, and business considerations for promotional materials and ensure adherence to CFR, FDA guidance, and PhRMA principles. This role develops strategies and mentors regulatory staff.

Hybrid schedule (3 days in office, 2 days remote) from AbbVie headquarters locations; requires leadership, strong communication, and deep experience in US advertising and promotion regulatory

Qualifications

• Bachelor’s degree in science plus 7 years of relevant industry experience (regulatory affairs, health authority, or ad promo).
• PharmD preferred with 5+ years in regulatory affairs and ad promo.
• Experience in a complex, matrix environment and strong negotiation skills.
• Excellent verbal and written communication; leadership experience preferred.
• US Regulatory Affairs Advertising and Promotion experience.

Responsibilities

• Capture and disseminate regulatory developments impacting AbbVie’s promotional policies.
• Represent department in trade associations and build relationships.
• Summarize findings in concise reports for AbbVie distribution.
• Oversee regulatory staff to ensure accurate, compliant advertising materials.
• Develop and guide implementation strategies for promotional activities.
• Ensure training and compliance with CFR, FDA guidelines, and SOPs.
• Present information to cross-functional groups and manage stakeholder communications.
• Foster relationships with Marketing, Legal, Medical, Sales Training, Public Affairs.

Skills

Communication skills

Negotiation

Management experience

Regulatory affairs

Education

Bachelor’s degree in science

PharmD degree

Job description

AbbVie in Irvine, CA seeks a Senior Manager Regulatory Affairs US Advertising and Promotion to lead regulatory, scientific, and business considerations for promotional materials and ensure adherence to CFR, FDA guidance, and PhRMA principles. This role develops strategies and mentors regulatory staff.

Hybrid schedule (3 days in office, 2 days remote) from AbbVie headquarters locations; requires leadership, strong communication, and deep experience in US advertising and promotion regulatory