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

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