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Senior Principal Scientist, Veterinary Pathology Board Certified

Merck
August 20, 2026
Full-time
Remote friendly (West Point, PA)
Worldwide
Clinical Research and Development
Role: Experienced anatomic pathologist specializing in toxicological pathology within a research-focused biopharma setting, contributing to safety assessments of drug candidates across early to late development stages. Responsibilities: perform routine and specialized postmortem evaluations, interpret data to characterize drug safety profiles, collaborate with multidisciplinary teams on mechanisms of toxicity, and support biomarker development. Lead or influence study designs and regulatory strategies, integrating advanced pathology tools such as digital pathology, immunohistochemistry, and electron microscopy. Qualifications: DVM required; PhD in Immunology, Toxicology, Pathology preferred; 10+ years’ experience in biotech, pharma, or CRO toxicology/pathology, with proficiency in histomorphology and GLP-compliant study analysis; board certification (ACVP/ECVP) essential. Preferred: expertise supporting immunology/biologics programs, experience leading pathology for drug development projects, and strong scientific leadership. High-Value: biologics, immunology, toxicology, GLP studies, biomarker discovery, safety evaluation, cross-functional collaboration, hybrid work environment, no travel required.