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Lead, coach, and develop Bioanalytical Study Management scientists as one integrated team, including goal setting, performance enablement, development planning, engagement, role clarity, and accountability for delivery; Set and drive the strategy for
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,
You will lead the development and execution of global regulatory strategies in close collaboration with co-development partners and internal and external stakeholders. Acting as regulatory lead for complex projects, you will draw upon
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