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
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📌 Principal Scientist/Study Director (Italia)
🏢 Altro
📍 Italia