Experteer Overview In this role you lead preclinical safety, PK and toxicology studies across rodent and non-rodent species. You own the entire study lifecycle from planning to data interpretation, coordinating internal and outsourced activities. You apply rigorous GLP/GRP practices and uphold ethical animal welfare standards. You contribute to methodological development and staff training, shaping trusted, high-quality preclinical science within a collaborative, fast-paced organization. Retribuzione / Benefits * Manage and coordinate preclinical safety, PK and toxicology studies in rodent and non-rodent species * Act as Study Director or Responsible Scientist overseeing the full study lifecycle * Perform in vivo tasks including treatments, sampling,



and clinical observations * Monitor outsourced preclinical studies at CROs to ensure quality and compliance * Develop new experimental methods and coordinate inter-laboratory activities * Draft operational procedures and SOPs * Support technical staff training and uphold animal welfare standards Responsabilità * Degree in Veterinary Medicine, Biology, or related field * Proven experience as a Study Director in toxicology and PK studies * Deep expertise in GLP and GRP regulations and their application * Skilled in in vivo techniques, sampling, and clinical observations * Background in monitoring outsourced studies and managing CROs * Strong ability to draft reports and standard operating procedures * Commitment to high animal welfare and ethical research standards #J-*****-Ljbffr

📌 Principal Scientist/Study Director (Torino)
🏢 Experteer Italy
📍 Torino