Full-Time Senior Director, Global RWE/HEOR Lead

The Senior Director, Global Real-World Evidence (RWE) and Health Economics and Outcomes Research (HEOR) Lead will be responsible for building and leading the function within medical affairs, and cultivating partnerships with cross-functional leaders in clinical development, program management, legal, regulatory, and commercial.

As an essential part of this growing organization, this role will oversee the strategy and execution of activities that are integral to developing and disseminating the clinical, humanistic, and economic value proposition of our therapies.

This role will work to ensure patients have maximized access to our therapies by generating and communicating evidence to support registration, inform healthcare decision-making, and appropriately educate payers on the value of our medicines.

Key Responsibilities include:

1. Create and lead the RWE/HEOR function within medical affairs
2. Develop comprehensive RWE/HEOR strategic plans and budgets for assets in development
3. Develop clinical, humanistic, and economic value propositions
4. Evaluate gaps in product value propositions and identify strategies to fill those gaps
5. Lead payer-focused research in the U.S. and ex-U.S. for feedback on product profiles, value propositions, evidence gaps, and evidence generation plans
6. Direct the design, conduct, and analysis of evidence-generating activities (economic models, chart reviews, etc.) to secure reimbursement or differentiate products
7. Collaborate with regulatory affairs on RWE activities for regulatory filings
8. Lead external dissemination of RWE/HEOR information (publications, presentations)
9. Engage with U.S. and ex-U.S. payers (including HTA submissions) to secure reimbursement
10. Be an integral part of internal teams for evidence-based decision-making
11. Oversee the development of a Global Value Dossier/AMCP Dossier
12. Identify, engage, and manage external partners (vendors)
13. Perform all activities in strict compliance with international regulations and industry best practices

Qualifications:

• Advanced degree (e.g., PharmD, PhD, or MD)
• Background in public health, health services research, epidemiology, health economics, or a related discipline
• Prior biopharmaceutical industry experience (10+ years preferred) in RWE/HEOR related oncology roles
• Experience launching therapies in oncology (U.S. required)
• Understanding of RWE/HEOR strategies and research methodologies
• Proven ability to develop strategic RWE/HEOR plans
• Familiarity with regulations addressing the use of RWE
• Proven ability to direct studies and model development
• Digital fluency and familiarity with applications for RWE/HEOR projects

Additional Information:

• Occasional business travel (~20%)

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