pIn this role, you will provide scientific, strategic and operational support across development activities, ensuring studies are designed and conducted in line with integral regulatory standards. You will act as a key scientific partner across RD, Regulatory Affairs, CMC and external partners, contributing to successful product development and lifecycle management. /ppstrongKey Responsibilities /strong /pulliLead the design of preclinical and clinical studies, defining objectives, endpoints and scientific rationale /liliOversee study protocols, analytical plans, reports and technical documentation /liliManage and collaborate with CROs, ensuring quality, compliance, timelines and budget adherence /liliEnsure GLP/GCP compliance and appropriate handling of study deviations and amendments /liliSupport regulatory submissions through preparation and review of scientific documentation /liliContribute to publications,



technical materials and lifecycle management activities /liliMaintain audit-ready documentation and support inspections and due diligence activities /liliMonitor scientific and regulatory developments and contribute to continuous improvement initiatives /li /ulpstrongWhy Animalcare? /strong /ppYou will join an international, science-driven organisation where collaboration, ownership and innovation are key. This is an opportunity to play a central role in developing products that make a real difference in animal health worldwide. /ppstrongbrPlease note /strong: Due to the high volume of applications we may receive, we might not be able to respond to each one. We appreciate your understanding and thank you for your interest. /ppAnimalcare Group is an equal opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all employeesbr/ppApply via LinkedIn and help us advance animal health through science and innovation. /p #J-18808-Ljbffr

📌 Clinical Development Manager EU-based (UK, Germany, Belgium, Portugal, Italy, Spain) (Barcelona)
🏢 Ecuphar
📍 Barcelona