• Provide senior oversight of PopPK, PBPK, PK/PD, exposure–response, and other quantitative pharmacology activities, including critical review of vendor outputs, assumptions, and conclusions. • Ability to critically review and challenge modeling outputs, study reports, analyses, assumptions, and conclusions, even when analyses are performed by external experts. • Strong scientific writing, communication, and stakeholder-management skills, with the ability to explain complex clinical pharmacology and DMPK topics clearly to cross-functional teams and senior decision-makers.
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