Global Regulatory Ad Promo Lead

Arrowhead Pharmaceuticals Canada

Pasadena (CA)

On-site

USD 180,000 - 240,000

Full time

7 hours ago
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Job summary

Arrowhead Pharmaceuticals, Inc. in Pasadena, CA is seeking an Associate Director/Director of Regulatory Affairs focused on Advertising and Promotion. This role leads US promotional review, advises on strategy, and manages FDA submissions across multiple channels.

The ideal candidate has 7+ years in Regulatory Affairs, strong MLR experience, and familiarity with PMR in other countries. A collaborative, risk-aware regulatory professional is essential to drive launches and policy improvements.

Qualifications

  • Bachelor’s degree in life sciences, pharmacy, regulatory affairs, or related discipline.
  • 7+ years in Regulatory Affairs Advertising & Promotion.

Responsibilities

  • Provide regulatory review and strategic guidance for US promotional materials across multiple channels.
  • Lead or participate in MLR meetings and provide risk-based regulatory recommendations.
  • Manage FDA submissions (OPDP/APLB) including 2253 submissions for US promotional materials.
  • Monitor FDA enforcement trends and industry developments to advise stakeholders.
  • Support launch readiness activities and continual policy improvements.
  • Collaborate across functions to ensure timely, compliant material development and approvals.

Skills

Regulatory affairs
FDA-OPDP regulations
MLR processes
PMR knowledge globally
Veeva PromoMats
Promotional materials review
Cross-functional collaboration

Education

Bachelor’s degree in life sciences/pharmacy/regulatory affairs

Tools

Veeva PromoMats

Job description

Arrowhead Pharmaceuticals, Inc. in Pasadena, CA is seeking an Associate Director/Director of Regulatory Affairs focused on Advertising and Promotion. This role leads US promotional review, advises on strategy, and manages FDA submissions across multiple channels.

The ideal candidate has 7+ years in Regulatory Affairs, strong MLR experience, and familiarity with PMR in other countries. A collaborative, risk-aware regulatory professional is essential to drive launches and policy improvements.

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