Sr. Director, Health Economics Outcome Research & Real-World Evidence
Taiho Oncology, Inc.
Summary
The Senior Director, HEOR/RWE provides strategic leadership for the development of integrated health economics, outcomes research and real-world evidence strategies across Taiho's portfolio. The role establishes evidence priorities from clinical development through launch and lifecycle management, ensuring robust clinical, economic and patient-centered evidence supports product value, medical strategy and stakeholder decision-making. The Senior Director serves as a senior HEOR/RWE subject-matter expert and strategic partner to Medical Affairs, Clinical Development, Market Access, Commercial and global stakeholders.
Job description
Position Summary
The Senior Director, HEOR/RWE provides strategic leadership for the development of integrated health economics, outcomes research and real-world evidence strategies across Taiho's portfolio. The role establishes evidence priorities from clinical development through launch and lifecycle management, ensuring robust clinical, economic and patient-centered evidence supports product value, medical strategy and stakeholder decision-making. The Senior Director serves as a senior HEOR/RWE subject-matter expert and strategic partner to Medical Affairs, Clinical Development, Market Access, Commercial and global stakeholders.
Performance Objectives
- Provide strategic leadership and accountability for integrated HEOR/RWE strategies and evidence-generation plans across assigned products and the broader portfolio.
- Establish portfolio and asset-level evidence priorities aligned with clinical development, Medical Affairs, Market Access and lifecycle objectives.
- Lead real-world evidence generation and health economic research designed to demonstrate the clinical, economic and patient-centered value of Taiho products.
- Provide senior-level HEOR/RWE input into clinical development programs, including study design, endpoints, patient-reported outcomes, evidence gaps and payer-relevant evidence requirements.
- Critically evaluate HEOR/RWE study designs, analyses and results and ensure scientific rigor, quality and appropriate interpretation.
- Oversee development of value evidence deliverables, including dossiers, economic models, evidence syntheses, abstracts, posters, manuscripts, presentations and other scientific communications.
- Provide strategic oversight of submissions to clinical compendia, pathways and payer/government organizations, as appropriate.
- Represent HEOR/RWE in senior cross-functional governance forums and at external scientific, payer, clinical and business meetings; influence evidence-based decisions across functions.
- Partner with Medical Field leadership and direct HEOR/RWE training and ensure field medical teams can appropriately understand and communicate value evidence.
- Provide strategic oversight of HEOR/RWE budgets, external vendors, research partnerships, timelines and resource prioritization across programs.
- Build effective relationships with alliance partners and global stakeholders to drive alignment of evidence strategies and deliverables.
- Provide functional leadership, coaching and scientific guidance to HEOR/RWE colleagues and matrix team members; directly manage staff where assigned.
- Monitor evolving HEOR methods, RWE standards, payer evidence expectations and healthcare policy and incorporate relevant developments into evidence strategy.
Education/Certification Requirements
Doctoral degree (Ph.D., Pharm.D., M.D., DrPH or equivalent) in health economics, outcomes research, epidemiology, health services research, public health or a related discipline strongly preferred; a relevant master's degree with substantial applicable experience may be considered.
Knowledge, Skills, and Abilities
- 10+ years of relevant HEOR/RWE experience in the pharmaceutical, biotechnology or related life sciences industry, with demonstrated progression in strategic responsibility.
- Demonstrated ability to develop and lead HEOR/RWE strategies across clinical development, launch and lifecycle management.
- Strong expertise in epidemiology, RWE, health economics, outcomes research, patient-reported outcomes and evidence-generation methodologies.
- Oncology, hematology and/or rare disease experience strongly preferred.
- Demonstrated ability to influence senior stakeholders and lead effectively in complex global and matrix environments.
- Strong scientific judgment and expertise in interpreting clinical, economic and real-world data.
- Experience overseeing publications, scientific communications, external research partnerships and vendors.
- Strong people leadership, coaching and matrix leadership capabilities.
- Excellent presentation, written and verbal communication skills, including the ability to translate complex evidence for diverse stakeholders.
- Ability to manage multiple strategic priorities, budgets and resources in a dynamic environment.
- Proficiency with Microsoft Office applications and relevant HEOR/RWE research tools and data sources.
- Ability to travel domestically and internationally, including occasional weekends, as business needs require.
Requirements
- 10+ years of relevant HEOR/RWE experience in the pharmaceutical, biotechnology or related life sciences industry
- Demonstrated ability to develop and lead HEOR/RWE strategies across clinical development, launch and lifecycle management
- Strong expertise in epidemiology, RWE, health economics, outcomes research, patient-reported outcomes and evidence-generation methodologies
- Demonstrated ability to influence senior stakeholders and lead effectively in complex global and matrix environments
- Strong scientific judgment and expertise in interpreting clinical, economic and real-world data
- Experience overseeing publications, scientific communications, external research partnerships and vendors
- Strong people leadership, coaching and matrix leadership capabilities
- Excellent presentation, written and verbal communication skills
- Ability to manage multiple strategic priorities, budgets and resources in a dynamic environment
- Proficiency with Microsoft Office applications and relevant HEOR/RWE research tools and data sources
- Ability to travel domestically and internationally, including occasional weekends
- Doctoral degree (Ph.D., Pharm.D., M.D., DrPH or equivalent) in health economics, outcomes research, epidemiology, health services research, public health or a related discipline strongly preferred
- Oncology, hematology and/or rare disease experience strongly preferred
Benefits
- Annual Bonus/Incentive Compensation
- Long-Term Incentive Plan
- 401(k)
- Paid Vacation
- Sick Time
- Parental Leave
- Medical Benefits
- Financial Benefits
Company overview
Taiho Oncology, Inc. is a specialized oncology pharmaceutical company focused on developing and commercializing innovative oral anti-cancer therapies. Founded in 2002 and headquartered in Princeton, New Jersey, the company operates as a subsidiary of Taiho Pharmaceutical Co., Ltd., which is part of Otsuka Holdings Co., Ltd. Taiho Oncology's mission is to improve the lives of patients with cancer, their families, and caregivers through the advancement of novel cancer treatments. The company specializes in orally administered anti-cancer agents targeting various tumor types, with a robust pipeline of small molecule clinical candidates for both solid tumors and hematological malignancies. Taiho Oncology has established a world-class clinical development organization and built a commercial business in the United States, while also overseeing its parent company's European and Canadian operations. The company's approach focuses on bringing novel technology to cornerstone chemotherapies for a wide range of tumor types, including colorectal cancer and other solid tumors. With approximately 201-500 employees, Taiho Oncology maintains operations in Princeton, New Jersey and Pleasanton, California, demonstrating its commitment to advancing oncology research and patient care through innovative pharmaceutical development.