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experience in integrated evidence generation plan (IEGP) development, RWE generation, HEOR strategy and analytics, health technology assessment, value dossier development, and payer engagement. Year 2 consists
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interactions, and reviewing tables, figures, and listings (TFLs). Responsible for analytical support of clinical trial data (safety and efficacy), including gathering, analyzing, reviewing, interpreting, and
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-functional collaboration with teams including US Marketing, Global Value & Access, Medical Affairs, Regulatory Affairs, Legal, Sales, and Insights & Analytics. The fellow will gain key experiences and skills
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partnering closely with the broader multi-functional USMA team including market access operations, pricing and contracting, analytics, and field teams. Additionally, the fellow will collaborate with critical
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, including Medical Affairs, Legal, Regulatory, Patient Services, Market Access, Data & Analytics, Market Insights, Competitive Intelligence, Global Marketing, and US Commercial Field teams to support
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, analyte binding, environmental responsiveness) to meet device requirements. This provides a unique opportunity to iteratively couple materials design with device performance. This position offers
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, and analysis Knowledge of or interest in principles and practices of evaluation and assessment Strong analytical skills Excellent time management skills Mature and professional approach to work Team
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, behavioral economics, or a related social science discipline (completed no later than August 2026) Strong analytic and theoretical skills, with experience in survey, qualitative, and mixed-methods research
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and/or issues and apply analytical and creative thinking to maximize performance. · Excellent written and verbal communication skills as well as organizational and project management skills
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, computational medicine, predictive analytics, big data, neuroscience, and related fields. AI + Life Sciences: Participate in research projects that are related to AI and the life sciences. These may include