Associate Principal Scientist, Toxicology/Study Director

Role: Senior Toxicologist serving as Study Director or Monitor within Nonclinical Drug Safety, leading and overseeing GLP and non-GLP toxicity studies across all modalities. Responsibilities: ensure study compliance, analyze and interpret data, integrate findings for regulatory submissions, and contribute to scientific leadership and cross-functional collaborations. Requirements: Master's in toxicology, pharmacology, or related field; minimum 8 years of relevant experience, with at least 5 years as a Study Director in pharma, biotech, or CRO; strong knowledge of GLP (US FDA 21 CFR Part 58). High-Value: expertise in general toxicology, GLP study directing, and familiarity with biologics and small molecules; experience with outsourced study monitoring and ICH safety guidelines preferred. Work setup: not specified; travel not required.