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Extrapolation (where appropriate), dose selection, trial design, PIP development and ongoing evaluation of data as generated. Transform PBPK and QSP analyses into actionable insights and communicate these findings effectively to project teams and
Transfer, optimize, and develop bioanalytical methods to support product development and quality control. Plan, execute, and document method pre-validation studies in accordance with applicable regulatory requirements. Authoring of Standard Operating
Responsible for leading non‑clinical and early clinical pharmacology strategy across drug development programs. Provides expertise in PK/PD, modeling & simulation, and Model‑Informed Drug Development (MIDD) to support dose selection, study design, and