Назад
Company hidden
7 дней назад

Senior Director, Health Economics & Outcomes Research (HEOR) (Rare Disease Biotech)

Формат работы
onsite
Тип работы
fulltime
Грейд
senior/director
Английский
b2
Страна
US
Вакансия из списка Hirify.GlobalВакансия из Hirify Global, списка международных tech-компаний
Для мэтча и отклика нужен Plus

Мэтч & Сопровод

Для мэтча с этой вакансией нужен Plus

Описание вакансии

Текст:
/
TL;DR
Senior Director, Health Economics & Outcomes Research (HEOR) (Rare Disease Biotech): Leading payer evidence strategies and patient-relevant outcomes research for early-stage rare disease assets with an accent on health technology assessment, market access, and clinical development alignment. Focus on designing patient-reported outcome strategies, guiding endpoint planning, engaging HTA agencies, and generating evidence for value demonstration and patient access.

Location: San Rafael, California, United States

Company

hirify.global is a rare disease biotechnology company developing therapies for genetically defined conditions.

What you will do

  • Lead payer evidence strategies and patient-relevant outcomes strategies for early-stage pipeline assets.
  • Align outcomes requirements with clinical development, regulatory, health technology assessment, and market access needs.
  • Direct patient-relevant endpoint planning and oversee implementation in clinical trials.
  • Develop Joint Clinical Assessment strategies and assess access implications across markets.
  • Lead research involving patient-reported outcome development and validation, health state valuation, and patient preference studies.
  • Engage with HTA agencies, regulators, payers, patient organizations, and internal cross-functional stakeholders to strengthen value propositions.

Requirements

  • 12+ years of pharmaceutical industry experience, including 7+ years in HEOR and at least 5 years in patient-relevant outcomes research.
  • Advanced degree in health economics, outcomes research, epidemiology, public health, health services research, pharmacy, or a related scientific discipline.
  • Deep understanding of market access, value, and global HTA frameworks.
  • Experience developing and validating patient-reported outcome measures, supporting HTA submissions, value dossiers, and patient-relevant briefing books.
  • Ability to lead complex initiatives and align senior stakeholders across Value & Access, Commercial, Medical Affairs, Clinical Development, and Regulatory Affairs.
  • Experience engaging HTA agencies, payers, health economists, clinical experts, and patient advocacy organizations.

Nice to have

  • Rare disease experience.
  • People leadership experience, including talent development.

Culture & Benefits

  • Work within global teams focused on developing therapies for patients with rare genetic conditions.
  • Collaborate across commercial, medical, clinical, regulatory, patient advocacy, and value and access functions.
  • Contribute to environmental protection, injury prevention, and workplace safety initiatives.

Будьте осторожны: если работодатель просит войти в их систему, используя iCloud/Google, прислать код/пароль, запустить код/ПО, не делайте этого - это мошенники. Обязательно жмите "Пожаловаться" или пишите в поддержку. Подробнее в гайде →