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21 час назад

Director US Advertising and Promotion Global Regulatory Affairs

178 500 - 257 833$
Формат работы
hybrid
Тип работы
fulltime
Грейд
director
Английский
b2
Страна
US
Вакансия из списка Hirify.GlobalВакансия из Hirify Global, списка международных tech-компаний
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Описание вакансии

Текст:
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TL;DR
Director US Advertising and Promotion Global Regulatory Affairs (Pharmaceutical Regulatory Affairs): Developing regulatory strategies for marketed and pipeline pharmaceutical products, overseeing US advertising and promotion activities, and liaising with the FDA with an accent on product labeling, promotion compliance, and cross-functional regulatory leadership. Focus on interpreting evolving regulations, managing product support projects, mentoring regulatory staff, and guiding complex promotion-related decisions.

Location: Morristown, New Jersey, or Cambridge, Massachusetts; US and Puerto Rico residents only. Hybrid work.

Salary: $178,500–$257,833.33 annually

Company

hirify.global is an R&D-driven, AI-powered biopharmaceutical company developing medicines and vaccines based on immunoscience.

What you will do

  • Provide strategic direction and oversee day-to-day regulatory activities for assigned products and departmental work.
  • Develop US regulatory strategies for product advertising, promotion, labeling, and product defense.
  • Provide senior regulatory guidance during issue management and evaluate the business impact of new regulations, guidance, and enforcement trends.
  • Maintain relationships with relevant FDA staff and collaborate with Commercial, R&D, Communications, Compliance, Legal, and Medical teams.
  • Mentor US Advertising and Promotion staff and support consistent policy application across assigned products.
  • Manage product support projects, priorities, timelines, and cross-functional participation.

Requirements

  • Bachelor’s degree from an accredited four-year college or university; a science focus is preferred.
  • Experience in pharmaceutical or medical device Regulatory Affairs, including Advertising and Promotion.
  • 8+ years of relevant regulatory experience.
  • Extensive knowledge of complex medical and scientific subject matter, the US pharmaceutical market, and medical terminology.
  • Strong strategic decision-making, communication, writing, relationship-building, and cross-functional collaboration skills.
  • Experience managing others is preferred; professional integrity and ethical judgment are required.

Culture & Benefits

  • Supportive, future-focused environment with opportunities for promotion, lateral career moves, and international development.
  • Rewards package with health and wellbeing benefits, healthcare, prevention and wellness programs, and at least 14 weeks of gender-neutral parental leave.
  • Work at the intersection of drug discovery, AI, data, and digital platforms.
  • Equal opportunity workplace committed to an inclusive workforce.

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