Scientific Director, Clinical Pathology

Role: Scientific Director in Clinical Pathology at Bristol Myers Squibb, focusing on interpretation and integration of clinical pathology data from nonclinical safety studies for biopharmaceutical development. Responsibilities include advising on study protocols, preparing regulatory reports, reviewing toxicology studies, providing expert consultation on complex findings, and supporting laboratory and methodology optimization. Qualifications: DVM, MS or PhD, and ACVP certification (or eligibility); 8+ years of industry or CRO experience interpreting clinical pathology from nonclinical studies; strong regulatory, GLP, and comparative pathology expertise; excellent communication and leadership skills. HighValue: expertise across diverse nonclinical species, contribution to product registration and regulatory submissions, and knowledge of GLP in a biopharma setting. Collaboration involves working with New Brunswick clinical pathology labs and multifunctional toxicology teams. Location: New Brunswick, NJ, with an emphasis on scientific leadership and innovation; work setup not explicitly specified.