Under the guidance of a senior leader, a Senior Principal Scientist/Senior Director, has primary responsibility for developing value evidence strategies, and planning/managing real world and economic evidence activities in the ophthalmology area to meet the value evidence needs of clinicians, payers, policymakers, HTA/reimbursement agencies and health systems globally. The ability to participate and lead cross-functional teams is a critical part of this role. This position may have people management responsibility. Types of studies executed include prospective and retrospective observational studies to characterize disease burden and epidemiology, treatment patterns, healthcare resource utilization and costs, physician and patient satisfaction surveys, clinical and patient reported outcomes assessments, systematic reviews and meta-analyses, and economic modelling. Key responsibilities also include development of American Managed Care Pharmacy (AMCP) dossiers for US payers, and Global Value Dossiers for use by local subsidiaries in their HTA submissions. Incumbent is also expected to contribute to product development and marketing strategies throughout the lifecycle to ensure that product value is defined and developed to achieve optimal market/patient access and reimbursement. The incumbent is expected to work cross-functionally with clinical development, medical affairs, biostatistics, market access, commercial and country affiliates and may have direct interactions with health technology assessment (HTA) agencies, reimbursement decision makers and national immunization technical advisory groups.
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Job Type
Full-time
Career Level
Senior
Industry
Chemical Manufacturing
Education Level
Ph.D. or professional degree