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environmental exposures and neurodevelopmental, behavioral, or health outcomes in children Knowledge of causal inference methods (e.g., propensity score analysis, directed acyclic graphs, mediation analysis
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which span across the key scientific pillars including; Patient-focused drug development including patient-reported outcomes as key measures in clinical trials Real-world evidence generation and analysis
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evidence plans across therapeutic areas Contribute to the design and execution of RWE and HEOR studies, including concept documents, protocols, statistical analysis plans, and study reports Contribute
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analysis of inquiry volume and trend metrics Provide training on the assigned product/disease area to contact center staff, Medical Affairs vendor partners, and Field Medical teams Support the development
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internal forums Support signal detection and management activities with Lead Safety Physicians and PV Scientists Engage in safety data review, analysis, and reporting of safety data to internal and external
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visits • Supporting business development activities, including product profile evaluation, competitive landscape analysis, and disease state research • Assisting with review and approval processes
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pharmacology lead and provide clinical trial operations support • Conduct noncompartmental PK analysis • Author clinical pharmacology sections of clinical study reports and provide support to regulatory
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analysis of competitive dynamics that may impact coverage, pricing, reimbursement & channel design Cross-functional collaboration with US Marketing, Global Value & Access, and Medical Affairs to ensure
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; Experience with EEG signal processing and study design; Statistical analysis skills for brain analyses; and Strong communication skills and ability to work both within a team and independently. KEY
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of Global Medical Affairs, develop skills in the analysis, interpretation, and communication of clinical data, and expand their scientific knowledge to render clinical insights and contribute to meeting the