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Provide PM expertise and leadership in model-informed drug development (MIDD) setting for all therapeutic areas in clinical study design (including dose rationales), data analyses to learn dose-exposure-response relationships and their variabilities, result interpretations and reporting Supervise and work with pharmacometricians and clinical pharmacologists in conducting PK (and/or PD) analysis (, to integrate all regional data and investigate ethnic differences) for regulatory submissions in China Engage with management, regional and global (internal and external including regulatory) stakeholders to drive MIDD strategies at project and portfolio levels Establish best practices for M&S pr...
About the Role
Summary
Lead the pharmacometrics (PM) group of ~6 members to support global and/or regional development projects, ensuring all modeling and simulation (M&S) deliverables are based on science with high quality and timeliness.
Responsibilities
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