Overview
In this role you will lead asset-specific payer evidence strategies to strengthen BioMarin’s access and value proposition across therapeutic areas. You will shape patient-relevant outcomes requirements within clinical programs and align them with Regulatory, HTA, and access needs. You will partner with cross-functional teams and external stakeholders to design, execute, and communicate outcomes research that differentiates BioMarin assets in the market. This position offers a chance to influence early access decisions and publish impactful research, contributing to patient access for rare diseases.
Responsibilities
- Lead development, execution and communication of payer evidence strategies aligned with brand priorities for early-stage assets
- Collaborate with Value & Access, Commercial, Medical Affairs, Clinical Development, Regulatory Affairs and Patient Advocacy organizations
- Drive understanding of payer and HTA requirements related to patient-relevant outcomes and health utility measurement
- Oversee asset-specific patient-relevant outcomes strategies informed by disease models
- Lead patient-relevant endpoint planning and trial implementation oversight
- Lead early Joint Clinical Assessment strategy development across markets
- Identify payer evidence gaps and inform integrated evidence planning for pipeline assets
- Manage external partnerships for PRO development, health state valuation, and patient preference research
- Lead scientific interactions with HTA agencies (EU HTA JSC, NICE, CADTH) including briefing materials and evidence packages
- Support regulatory and patient advocacy interactions and communicate value through integrated evidence plans
- Shape exploration and interpretation of trial outcomes data to strengthen HTA and payer value propositions
- Develop strategic scientific communications and publish research in peer-reviewed journals
- Assess BD opportunities against payer/HTA requirements to identify risks and gaps
- In partnership with IET, analyze patient-relevant outcomes data to generate insights for stakeholders
Key requirements
- 12+ years in pharma with 7+ years in HEOR or related roles
- 5+ years direct experience with patient-relevant outcomes research
- Advanced degree in health economics, outcomes research, epidemiology, public health, health services research, pharmacy or related field
- Deep understanding of market access, value and global HTA frameworks
- Proven experience developing and executing patient-relevant outcomes strategies
- Experience in evaluation, development, and validation of PRO measures for regulatory, payer, and HTA decision making
- Experience supporting HTA submissions, value dossiers, and patient-relevant briefing books
- Proven ability to influence across senior cross-functional stakeholders
- Ability to manage multiple complex initiatives in a fast-paced environment
- Leadership experience and external visibility in the PRO field
- Experience engaging with HTA agencies, payers, health economists, experts, and patient organizations
- Rare disease experience preferred
- People leadership experience preferred
- influencing and negotiating with senior stakeholders
- cross-functional collaboration
- strategic thinking and prioritization
- HEOR strategy
- PRO development and validation
- HTA submissions and value dossiers
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