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3 дня назад

Senior Enterprise Policy Development Manager (Life Sciences)

127 100 - 152 332$
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 Enterprise Policy Development Manager (Life Sciences): Developing and managing evidence-based policy statements, white papers, journal articles, presentations, and formal comments for public health and regulatory stakeholders with an accent on scientific rigor, drug regulation, and cross-functional collaboration. Focus on convening stakeholders, building evidence-based partnerships, and delivering complex policy projects aligned with global external affairs priorities.

Location: Rockville, Maryland, United States

Salary: USD $127,100–$152,332 annually, plus a target annual bonus that varies by role level.

Company

hirify.global is an independent scientific organization developing quality standards for medicines, dietary supplements, and food ingredients through global collaboration.

What you will do

  • Develop and manage evidence-based enterprise policy content, including public policy statements, white papers, journal articles, presentations, and formal comments.
  • Partner with scientific, public health, and external affairs colleagues to support policy priorities and informed stakeholder dialogue.
  • Convene internal and external stakeholders, gather perspectives, and build alignment around policy content and program priorities.
  • Cultivate collaborations with academic institutions, consultants, and other external partners.
  • Develop programs, forums, and communications that increase awareness and use of policy content.
  • Deliver 3–4 major projects annually within established deadlines.

Requirements

  • Bachelor’s degree in a relevant field.
  • Very strong writing skills and experience developing substantive policy materials for varied audiences.
  • Ability to learn new information rapidly and build credibility with stakeholders.
  • Demonstrated ability to collaborate across functions, build consensus, and meet deadlines in a fast-paced environment.
  • Some familiarity with drug development and regulation.
  • Onsite role based in Rockville, Maryland, United States.

Nice to have

  • Advanced degree in public policy, public health, law, science, medicine, or a related field.
  • Progressively responsible experience in life sciences, public health, public policy, regulatory affairs, government, nonprofit, or related sectors.
  • Experience with biological product research or development and complex stakeholder projects.
  • Knowledge of international regulatory frameworks, trade policy, supply chains, AI applications in quality frameworks, environmental sustainability, or advanced manufacturing.
  • Public speaking experience and experience working with international stakeholders.

Culture & Benefits

  • Mission-driven work focused on improving global access to high-quality medicines and health products.
  • Inclusive and collaborative environment centered on scientific integrity, fairness, and equitable participation.
  • Company-paid time off and comprehensive healthcare options.
  • Retirement savings benefits and leadership and workforce development programs.

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