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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
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