Senior Manager RA US Advertising and Promotion - Hybrid

Responsibilities:
- Proactively track and share government, industry, and trade association activities impacting pharmaceutical regulatory policies; draft/finalize regulator and trade association comments.
- Represent the department in trade associations; build relationships with trade association managers.
- Summarize findings into concise reports (under supervision).
- Oversee productivity/development of regulatory staff ensuring advertising and promotion materials are accurate, competitive, and compliant with CFR, FDA guidance, PhRMA Guiding Principles, and applicable FDA/cosmetic law.
- Develop and guide implementation strategies for promotional activities.
- Apply regulatory/technical knowledge across therapeutic areas.
- Ensure training and compliance for advertising/promotion regulations, guidance, promotional guidelines, and SOPs; manage direct reports and support hiring, training, and mentoring.
- Present information to cross-functional groups and deliver difficult messages without harming relationships.
- Establish relationships with key stakeholders (Marketing, Medical, Clinical, Legal, Sales Training, Managed Care, Public Affairs, etc.).
- Hybrid schedule: 3 days in office/2 days remote from Lake County, IL; Florham Park, NJ; or Irvine, CA.

Qualifications:
- Minimum: Bachelor’s degree in science plus 7 years relevant industry experience (regulatory affairs fellowship, Health Authority, ad promo, etc.).
- Preferred: PharmD plus 5 years relevant experience.
- Experience in complex matrix environments; strong negotiation; strong oral/written communication.
- Experience in US Regulatory Affairs Advertising and Promotion; management experience preferred.

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

Significant Work Activity:
- Continuous sitting for prolonged periods (>2 consecutive hours in an 8-hr day)