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Associate Director, Global Regulatory Affairs-Advertising and Promotion Review Lead

Takeda
Full-time
Remote friendly (United States)
United States
Medical Affairs

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Role Summary

Associate Director, Global Regulatory Affairs Advertising and Promotion Review Lead. Responsible for management of assigned programs/products as the internal expert on US Codes, guidance, and industry standards pertaining to prescription medicine promotion, supporting the Oncology Portfolio.

Responsibilities

  • Serve as GRA A&P SME for assigned products and projects.
  • Regulatory advisor as the β€œR” in the core Medical, Legal, Regulatory review functions of the Commercial Material Review Process (CMRP) and Medical Material Review Process (MMRP) for both Commercial and Medical material development, review, approval, and implementation
  • Product or project business lead for global CMRP at Takeda
  • CMRP Meeting Chair- pausing to communicate comments to coordinator, diffusing team disputes, serving as a dependable negotiator, keeping the team focused on patients, and overseeing escalation steps if MLR cannot align or if new data or campaigns require senior input
  • Strategic business partner from clinical trial development through the marketing maintenance phase of a product lifecycle
  • Subject matter expert on FDA code/regs, guidance, industry standards, complaints/violations, and innovative promotional platforms with additional training on International Codes and guidelines for Global product support
  • Partner closely with line-management, Oncology GRA A&P Portfolio Lead and inform or bring in Head of GRA A&P for complex review concepts or topics
  • Empowered decision-maker within the CMRP

Qualifications

  • Bachelor's Degree in a science-related field is required.
  • Master's Degree preferred. Minimum of 3 years’ experience required in material review and approval process of pharmaceutical/biologics promotion.
  • Ability to understand ABPI, EFPIA and other international code and guidance about advertising and promotion for prescription medicines.
  • Experience in prescription medicine promotion development and review process.
  • Strong interpersonal skills with ability to demonstrate strategic and analytic thinking.
  • Demonstrated ability to communicate clearly and concisely.
  • Highly effective written and verbal communication skills to manage, motivate and drive decisions within teams.
  • Proven skills in negotiation, influencing without authority and working diplomatically through conflict.
  • Demonstrated cross-functional people management with a desire to foster a positive team culture.
  • Ability to work independently, take initiative and complete tasks to deadlines.
  • Previous experience in an advertising and promotion role.
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