7 дней назад
Senior Director, Health Economics & Outcomes Research (HEOR) (Rare Disease Biotech)
Мэтч & Сопровод
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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
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.
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