• Develop integrated clinical pharmacology, DMPK, ADME, PK/PD, and model-informed development plans to support dose selection, study design, safety assessment, and regulatory submissions. • Interpret clinical and nonclinical pharmacology, PK, safety, exposure–response, and modeling data and translate them into pragmatic, regulatorily defensible development decisions. • Proven ability to interpret clinical and nonclinical pharmacology, PK, safety, exposure–response, and modeling data and translate them into clear, pragmatic, and regulatorily defensible development recommendations. • Ability to critically review and challenge modeling outputs, study reports, analyses, assumptions, and conclusions, even when analyses are performed by external experts.
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