Principal Scientist/Study Director

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