Regulatory Affairs: Advertising & Promotion Leader

BioSpace

Cambridge (MA)

Presencial

USD 130 000 - 170 000

Tempo integral

há 13 horas
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Resumo da oferta

Sanofi is seeking a Manager Regulatory Affairs Advertising and Promotion in Cambridge, MA / Morristown, NJ. The role drives regulatory strategies for labeling, advertising, and promotion across products, partnering with brand teams and global counterparts.

You will contribute to risk/benefit analyses, guide cross-functional teams, and ensure compliant promotional practices within the US marketplace. A science background and 1+ year regulatory experience are preferred.

Qualificações

  • Bachelor's degree from an accredited four-year college or university; science focus preferred.
  • 1+ years experience in pharmaceutical or medical device Regulatory Affairs.
  • Experience with cross-functional groups including Medical, Legal, Marketing.

Responsabilidades

  • Identifies product-specific or therapeutic area A&P issues and collaborates to implement solutions.
  • Advises risk/benefit of strategies and guides clients in regulatory matters.
  • Oversees regulatory strategic objectives and projects with minimal supervision.
  • Acts as Regulatory representative on brand teams and review committees for commercial and medical materials.
  • Provides input to Global organization on domestic regulatory strategies for life-cycle management.
  • Contributes A&P expertise to labeling for new/ supplemental NDAs.
  • Delivers regulatory strategies to maximize value and balance risks for stakeholders.
  • Performs other duties as assigned.

Conhecimentos

Regulatory Affairs
Advertising & Promotion
Cross-functional teamwork
Regulatory strategy
Medical terminology

Formação académica

Bachelor's degree

Descrição da oferta de emprego

Sanofi is seeking a Manager Regulatory Affairs Advertising and Promotion in Cambridge, MA / Morristown, NJ. The role drives regulatory strategies for labeling, advertising, and promotion across products, partnering with brand teams and global counterparts.

You will contribute to risk/benefit analyses, guide cross-functional teams, and ensure compliant promotional practices within the US marketplace. A science background and 1+ year regulatory experience are preferred.

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