Co-leads development, delivery and communication of PCO reimbursement strategy within HTAP, IPAS, 1BP and aligned with Integrated Evidence Plan
Oversees one therapeutic area and supports multiple assets/indications
Ensures PCO measurement strategy includes patient reported outcomes and health utilities relevant for international HTAs and payers
Participates in and co-leads projects to include PCOs in clinical trials, non-interventional studies and real-world studies
Integrates local PCO requirements into global/international evidence plans and PCO activities
Leads health state valuation projects via development and management of Time Trade-Off (TTO) or Standard Gamble (SG) studies
Assists in scientific discussions with HTA agencies and prepares briefing documents and dossiers
Develops strategic scientific communication plans including submissions and presentations in peer-reviewed journals and congresses
Engages with external thought leaders and represents Novartis with external stakeholders
Leads above-brand research projects to pilot innovative methodologies and elevate internal standards
Cultivates partnerships with Access, Clinical Development, PCO COE, AQS Biostat, Medical Affairs and International Commercial organization
Requirements
8+ years of Pharma Industry experience
5+ years of experience in HEOR roles in pharmaceutical companies or consulting
At least 3 years demonstrating specific leadership of health utility projects
Advanced Degree in relevant field
Experience in evaluating, developing and validating PRO/PCO instruments to meet HTA reimbursement requirements
In-depth understanding of key patient centered outcomes measurement systems – e.g., EuroQoL, Quality Metric Short-Form measures, HUI etc.
Ability to lead in a cross functional environment
Ability to manage multiple priorities in rapidly changing environment
Ability to work collaboratively to leverage other HEOR capabilities (strategy, regions, countries, COE PCO)
Experience in conducting and evaluating PCO measures from conceptualization through negotiation with international health authorities (desirable)
Experience in HTA submissions (desirable)
Ph.D., M.D., MBA, MSc or equivalent (desirable)
Strong external interfaces and network: KOLs, clinical research & scientific groups, payers, and policy organizations (desirable)
Benefits
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