LIST RESPONSIBILITIES REQUIRED:   The Reproductive Toxicology Department is seeking a scientist with expertise in developmental and reproductive toxicology. Toxicologists at our company play an active role in the process of drug development from late stage discovery through marketed products. Working in a collaborative team environment, the successful candidate will design and direct monitor in vivo toxicology studies to support the goals of both biologics and small molecule project teams in compliance with ICH guidelines, partnering with pathologists and toxicokineticists to deliver high quality GLP and non GLP in vivo study reports and, as needed, represent the company in meetings with regulatory authorities. Responsibilities include interdisciplinary project team membership, preparation and review of regulatory documentation, study reports and manuscripts, participation in toxicology and pharmacology initiatives, and other active cross functional collaborations.

LIST MAJOR SKILLS REQUIRED:  Doctoral degree Ph.D. or equivalent training and experience specializing in developmental and reproductive toxicology, with 3 to 7 years experience directly involved in study conduct, data analysis and report authorship. Knowledge of regulatory and GLP guidelines in toxicology and reproductive toxicology is essential. Experience in drug development and toxicokinetics is highly desirable.

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