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You will be involved in the European Surveillance of Veterinary Antimicrobial Consumption (ESUAvet) activity, one of EMA's high-profile outputs supporting the fight against AMR. You will coordinate Member States’ data reporting contribute to data
Lead the design and execution of clinical pharmacology strategies and corresponding studies across multiple programs. Develop innovative and meaningful clinical pharmacology approaches that accelerate and de-risk drug development Define dose selection,
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