The incumbent will be responsible for providing pathology support to Research with additional contributions to preclinical safety assessment across the drug development process. This will include pharmacologic studies with morphologic endpoints . as well as regulatory toxicologic pathology studies. S/he is expected to contribute to lead optimization and mechanistic studies by applying morphological tools for assessment of molecular pathways. To that end, a current knowledge of recent advances and new equipment/procedures is important. The incumbent may be asked to peer review internal or external studies as needed. An ability to work in multidisciplinary teams within Preclinical Safety and Research/Development is a must. This position requires good verbal and written communication skills.DVM (or equivalent) and board certification by ACVP are required and a PhD in pathology is preferred. The candidate should have experience in toxicologic pathology/investigative pathology up to 10 years.

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