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Sanofi

Global pharma company; vaccines and R&D

Senior Manager Regulatory Affairs Advertising and Promotion

Regulatory & Quality (Life Sciences)Confirmed live in the last 24 hours
Full-time$122.3k - $176.6k

About the Job

Requirements

  • A bachelor's degree from an accredited four-year college or university is required; a science focus is preferred but not required.
  • At least 3 years of experience in pharmaceutical or medical device advertising and promotional review.
  • A successful track record, ideally including 1–3 years of relevant regulatory experience.
  • Experience working effectively with cross-functional groups, potentially including Medical, Legal, and Marketing.
  • Knowledge and understanding of complex medical and scientific subject matter.
  • Understanding of the U.S. pharmaceutical marketplace and familiarity with medical terminology.
  • Ability to compare data from different sources, draw conclusions, and choose an appropriate course of action or solution.
  • Ability to develop collaborative relationships and internal networks to gain cooperation and accomplish work goals.
  • Ability to propose innovative solutions to work problems and opportunities.
  • Ability to use appropriate interpersonal styles and techniques to gain acceptance of ideas or plans.
  • Professional ethics, integrity, and personal values consistent with the company's values.
  • Ability to balance projects with day-to-day duties, establish priorities and timelines, and manage workload and multiple tasks effectively.
  • Ability to represent information and data accurately and honestly.

Responsibilities

  • Independently review advertising, promotional, communications, and other materials, and help develop and implement regulatory strategies for promotional and advertising campaigns, including serving as regulatory lead for product launches.
  • Identify product-specific or therapeutic-area advertising and promotion issues and work with other teams to propose and implement solutions.
  • Identify strategies for addressing issues, advise on the risks and benefits of each, and assist clients in making business decisions with an understanding of potential regulatory risks and benefits.
  • Oversee and take responsibility for successful implementation of regulatory strategic objectives and projects with minimal supervision.
  • Participate actively as the Regulatory representative on brand teams and Review Committees for commercial and medical materials.
  • Provide guidance and feedback to internal commercial and R&D groups to maximize the competitive impact of product development and subsequent promotion, advertising, and reimbursement.
  • Provide input to the Global organization on domestic regulatory strategies for in-line products through lifecycle management programs.
  • Contribute advertising and promotion expertise to the development of optimal labeling for new and supplemental new drug applications.
  • Develop product-specific regulatory strategies to mitigate risk and work with brand-team management to provide advice and risk/benefit analysis to maximize value to stakeholders.
  • Serve as the primary liaison with the FDA for assigned products on advertising and promotional compliance matters.
  • Perform other duties as assigned.

Desired Qualifications

  • A science focus for the required bachelor's degree is preferred.
  • Relevant regulatory experience of 1–3 years is described as ideal.

About the Company

Sanofi

Global pharma company; vaccines and R&D

Sanofi is a global pharmaceutical and biotechnology company that develops, manufactures, and sells prescription medicines, over-the-counter products, and vaccines. Its products span immunology, oncology, rare diseases, and vaccines, addressing unmet medical needs through a strong focus on research and development. Sanofi's core product model relies on large-scale R&D, strategic partnerships, and licensing to bring new therapies to markets, with revenue generated from product sales and collaborations. The company differentiates itself by leveraging its global reach, diverse portfolio, and emphasis on patient-centric solutions, safety, and quality to navigate regulatory environments in developed and emerging markets. The company’s goal is to improve health outcomes and quality of life for people worldwide by delivering innovative treatments and vaccines that meet unmet medical needs.

Company size
10,001+
Company stage
IPO
Headquarters
Paris, France
Founded
1973

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