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21 минуту назад

Senior Manager, Regulatory Affairs Advertising and Promotion

122 250 - 176 583$
Формат работы
onsite
Тип работы
fulltime
Грейд
senior
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
Senior Manager, Regulatory Affairs Advertising and Promotion (Pharmaceutical Regulatory Affairs): Conducting independent reviews of advertising, promotional, communications, and medical materials while developing regulatory strategies for campaigns, product launches, labeling, and product defense with an accent on advertising compliance, FDA engagement, and risk-benefit analysis. Focus on leading cross-functional reviews, resolving complex promotional issues, and implementing regulatory objectives for pharmaceutical products.

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

Salary: $122,250–$176,583.33 per year, commensurate with experience.

Company

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

What you will do

  • Conduct independent regulatory reviews of advertising, promotional, communications, commercial, and medical materials.
  • Develop and implement regulatory strategies for advertising and promotion campaigns, including product launches.
  • Identify product-specific and therapeutic-area advertising and promotion issues and propose solutions.
  • Advise brand teams and internal commercial and R&D stakeholders on regulatory risks, benefits, and compliance strategies.
  • Represent Regulatory Affairs on brand teams and review committees and serve as the primary FDA liaison for assigned products.
  • Contribute advertising and promotion expertise to labeling strategies, new drug applications, product defense, and lifecycle management.

Requirements

  • Bachelor’s degree in Life Sciences from an accredited four-year college or university.
  • At least 3 years of experience, including pharmaceutical or medical device advertising and promotional review.
  • Ideally 1–3 years of relevant regulatory affairs experience.
  • Experience working effectively with cross-functional groups including Medical, Legal, and Marketing.
  • Knowledge of complex medical and scientific subject matter, medical terminology, and the U.S. pharmaceutical marketplace.
  • Strong oral and written communication, prioritization, multitasking, analytical, and collaborative skills, with professional integrity and ethical judgment.

Culture & Benefits

  • Work alongside a supportive, future-focused team focused on scientific innovation.
  • Opportunities for career growth through promotions and lateral or international moves.
  • Company rewards and employee benefit programs.
  • Healthcare, prevention, wellness, and family benefits.
  • At least 14 weeks of gender-neutral parental leave.

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