Study Director III, Toxicology

Role: Study Director responsible for overseeing all phases of preclinical study protocols in a GLP environment, including study design, staff supervision, and reporting. Responsibilities: develop protocols, coordinate study initiation, monitor progress, ensure regulatory compliance (cGMP/GLP), and prepare scientific reports and publications. Requirements: bachelor’s degree with 10+ years, master’s with 5+ years, or doctoral with 2+ years relevant experience in biological sciences; strong organizational, communication, and regulatory knowledge; proficiency in database tools. High-Value: preclinical studies, GLP compliance, biological sciences, regulatory adherence, study oversight. WorkSetup: unspecified, likely laboratory and office environment; no travel specified.