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5 дней назад

Senior Director, Patient Advocacy (Biotech)

216 100 - 360 200$
Формат работы
hybrid
Тип работы
fulltime
Грейд
senior/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
Senior Director, Patient Advocacy (Biotech): Building enterprise-wide patient advocacy strategy and governance across discovery, development, and commercialization with an accent on patient voice integration, cross-functional partnerships, and measurable patient impact. Focus on designing multi-year advocacy roadmaps, translating corporate priorities into therapeutic-area plans, and reporting KPIs through board-ready materials.

Location: Sleepy Hollow, New York, United States; hybrid with onsite work 4 days per week

Salary: $216,100–$360,200 annually

Company

hirify.global is a biotechnology company developing and commercializing medicines for serious diseases, including rare diseases, cancer, eye diseases, cardiovascular and metabolic conditions, and hematologic disorders.

What you will do

  • Shape enterprise-wide patient advocacy strategy across discovery, development, and commercialization.
  • Build standards and governance for engagement with patient advocacy and professional organizations.
  • Partner with Medical, Commercial, Market Access, Policy, and Clinical Development teams on a multi-year advocacy roadmap.
  • Drive faster diagnosis, stronger clinical-trial awareness, broader access, and improved patient experience.
  • Translate corporate priorities into therapeutic-area plans with clear decision rights.
  • Track external trends and policy changes, and report progress through KPIs, dashboards, and board-ready materials.

Requirements

  • Bachelor’s degree and 12+ years of relevant experience, including 10+ years leading multi-stakeholder patient advocacy programs.
  • Experience building enterprise-wide, cross-functional programs with measurable business impact.
  • Strong executive presence and communication skills, including preparation of board-ready materials.
  • Experience working with Medical, Commercial, Market Access, and Policy teams, with knowledge of advocacy compliance requirements.
  • Ability to lead through influence, structure ambiguity, and communicate complex work in a concise, data-driven manner.

Nice to have

  • Experience in rare disease, oncology, hematology, ophthalmology, immunology, or cardio-metabolic disease.
  • Experience in complex, matrixed, or global organizations.
  • Alliance management experience.

Culture & Benefits

  • Inclusive workplace and equal opportunity employment.
  • Comprehensive rewards may include annual bonuses, equity awards, retirement benefits, health and wellness programs, insurance, paid time off, and family support benefits.
  • Work is designed around collaboration and togetherness, with significant onsite expectations for this role.

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