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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
In this role you will provide scientific, regulatory, and procedural input and oversight relating to the safety, efficacy and quality aspects of veterinary medicines, specifically on referral procedures to the Agency’s Committee for Veterinary Medicinal
Utilize and establish advanced in vitro and in vivo models of ocular disease, and leverage available patient sample datasets to identify, validate, and characterize novel therapeutic drug targets; Independently lead and manage drug discovery projects from
Guide ICON project teams on clinical issues, ensuring studies adhere to the highest ethical principles and legal standards. Contribute to investigator meeting presentations, review study documentation, oversee safety data reviews and support Business
You will identify compliance gaps, guide investigations, and lead improvements that support reliable laboratory processes. You will also share your expertise and help teams prepare for regulatory inspections. Lead improvement projects with QC, Quality