Associate Director, Regulatory Affairs Advertising and Promotion

Job Summary

The Associate Director, Regulatory Affairs Advertising and Promotion (RAAP) provides strategic and tactical regulatory support for U.S. promotional and selected non‑promotional communications across assigned products, disease‑state initiatives, and related external‑facing materials within the Daiichi Sankyo portfolio. Reporting to the Head of RAAP, this role serves as a primary Regulatory reviewer and subject‑matter expert for assigned scope and helps ensure materials are developed, reviewed, and approved in accordance with FDA regulations, guidance, approved labeling, internal standards, and relevant regulatory precedent prior to dissemination.

The Associate Director provides practical, risk‑based regulatory guidance to cross‑functional stakeholders and supports compliant, business‑aligned promotional execution. This role is responsible for independent day‑to‑day review of assigned materials, participation in cross‑functional review forums, and contribution to review practices that improve consistency, efficiency, and transparency across the RAAP function.

The Associate Director applies established regulatory standards and precedent within assigned scope and escalates novel, high‑risk, or precedent‑setting matters to the Head of RAAP, as appropriate.

Responsibilities

• Provide regulatory review, guidance, risk assessment, and mitigation recommendations for branded and unbranded promotional materials to ensure compliance with FDA advertising and promotion requirements, approved labeling, internal policies, and company standards.
• Review a broad range of HCP‑ and patient‑facing promotional materials and assess them for consistency with prescribing information, fair balance, risk communication, evidentiary support, and relevant FDA/OPDP expectations.
• Apply current laws, regulations, guidances, enforcement trends, and regulatory precedent to assigned reviews and recommend practical, compliant solutions that support business objectives.
• Maintain current knowledge of evolving advertising and promotion requirements and communicate relevant regulatory developments and implications to stakeholders and colleagues.
• Participate in concept‑stage discussions and formal promotional review meetings to provide proactive, solution‑oriented, and risk‑based regulatory guidance during material development.
• Serve as the RAAP reviewer for assigned products and communications within PMRT and other cross‑functional review forums.
• Partner with Medical, Legal, Compliance, Commercial, Clinical, Labeling, Public Affairs, Corporate Communications, Market Access, and alliance partners to support aligned, efficient, and compliant review of promotional materials.
• Build effective working relationships with stakeholders and elevate significant regulatory issues, interpretive questions, or unresolved cross‑functional disagreements to RAAP leadership, as appropriate.
• Serve as a RAAP reviewer in promotional review committees and as a functional representative on the Labeling Working Team for assigned products and materials, as appropriate.
• Guide and support required promotional submissions, including Form FDA 2253, Subpart E/H, advisory comment submissions, and other regulatory filing activities.
• Support ad/promo interactions with OPDP and other regulatory authorities in partnership with RAAP leadership.
• Apply current FDA regulations, guidances, enforcement trends, compliance letters, and relevant regulatory precedent to assigned reviews, and elevate ambiguous, novel, or high‑risk interpretive issues as appropriate.
• Support implementation and reinforcement of consistent RAAP review practices, workflows, decision principles, and review expectations across assigned products and materials.
• Assist in development, maintenance, and application of internal procedures, standards, guidance documents, and review tools related to promotional review.
• Support continuous improvement efforts that enhance review quality, consistency, transparency, and efficiency across the RAAP function.
• Provide training and knowledge‑sharing for internal stakeholders on advertising and promotion requirements, enforcement trends, and company expectations.

Qualifications

• Education: Bachelor’s Degree in a scientific, healthcare, or related discipline required; PharmD, PhD, MS, MPH, or JD preferred.
• Experience: 7+ years relevant pharmaceutical or biotechnology industry experience in Regulatory Affairs, including direct support of U.S. advertising and promotion review preferred; 4+ years U.S. regulatory affairs advertising and promotion review experience in oncology with product launch experience required.
• Travel Requirements: In‑house office position that may require occasional travel.

Daiichi Sankyo, Inc. is an equal‑opportunity/affirmative action employer. Qualified applicants will receive consideration for employment without regard to sex, gender identity, sexual orientation, race, color, religion, national origin, disability, protected veteran status, age, or any other characteristic protected by law.

Salary Range: USD$166,720.00 – USD$250,080.00