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 xysqume 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 (Torino)
🏢 Experteer Italy
📍 Torino