Senior Manager, Regulatory Affairs US Advertising and Promotion - Immunology - Hybrid
AbbVie
August 22, 2026
Remote friendly (Florham Park, NJ)
United States
$124,500 - $236,500 USD yearly
Corporate Functions
Senior Manager Regulatory Affairs US Advertising and Promotion – Immunology
Responsibilities:
- Proactively monitor and disseminate government/industry/trade association activities impacting pharmaceutical regulatory policies; draft and finalize regulator/trade comments; distribute proposed policies to SMEs.
- Represent the department and participate in trade associations; build relationships with trade association managers.
- Summarize findings (under supervision) in concise reports for internal distribution.
- Oversee productivity and development of regulatory staff ensuring advertising and promotion materials are accurate, competitive, and compliant with internal policies and applicable regulations/guidance.
- Develop and guide implementation strategies for promotional activities.
- Apply regulatory/technical knowledge across therapeutic areas.
- Ensure training and compliance with advertising/promotion regulations, guidelines, and SOPs for self and direct reports; manage, develop, train, and mentor staff.
- Present information to cross-functional groups; deliver difficult messages to commercial teams without damaging relationships.
- Establish relationships with key stakeholders (Marketing, Medical, Clinical, Legal, Sales Training, Managed Care, Public Affairs).
- Hybrid schedule: 3 days in office, 2 days remote from Lake County, IL; Florham Park, NJ; or Irvine, CA.
Significant work activities: continuous sitting >2 consecutive hours in an 8-hour day.
Qualifications:
- Minimum: Bachelor’s degree in science plus 7 years relevant industry experience.
- Preferred: PharmD plus 5 years relevant industry experience.
- Experience in complex matrix environments; strong negotiation.
- Strong oral and written communication.
- Management experience preferred.
- Experience in US Regulatory Affairs Advertising and Promotion.
Benefits:
- Paid time off; medical/dental/vision insurance; 401(k); eligible for long-term incentive programs.
Responsibilities:
- Proactively monitor and disseminate government/industry/trade association activities impacting pharmaceutical regulatory policies; draft and finalize regulator/trade comments; distribute proposed policies to SMEs.
- Represent the department and participate in trade associations; build relationships with trade association managers.
- Summarize findings (under supervision) in concise reports for internal distribution.
- Oversee productivity and development of regulatory staff ensuring advertising and promotion materials are accurate, competitive, and compliant with internal policies and applicable regulations/guidance.
- Develop and guide implementation strategies for promotional activities.
- Apply regulatory/technical knowledge across therapeutic areas.
- Ensure training and compliance with advertising/promotion regulations, guidelines, and SOPs for self and direct reports; manage, develop, train, and mentor staff.
- Present information to cross-functional groups; deliver difficult messages to commercial teams without damaging relationships.
- Establish relationships with key stakeholders (Marketing, Medical, Clinical, Legal, Sales Training, Managed Care, Public Affairs).
- Hybrid schedule: 3 days in office, 2 days remote from Lake County, IL; Florham Park, NJ; or Irvine, CA.
Significant work activities: continuous sitting >2 consecutive hours in an 8-hour day.
Qualifications:
- Minimum: Bachelor’s degree in science plus 7 years relevant industry experience.
- Preferred: PharmD plus 5 years relevant industry experience.
- Experience in complex matrix environments; strong negotiation.
- Strong oral and written communication.
- Management experience preferred.
- Experience in US Regulatory Affairs Advertising and Promotion.
Benefits:
- Paid time off; medical/dental/vision insurance; 401(k); eligible for long-term incentive programs.