Senior Study Director, Preclinical Toxicology
Charles River
Charles River is seeking an experienced Study Director to oversee preclinical efficacy and/or toxicology studies, ensuring GLP compliance and timely reporting. You will design study plans, coordinate protocols, and interact with sponsors to align on study costs and schedules. The role covers study execution, data interpretation, and communication with internal teams and clients. Candidates should have a BA/BS in toxicology or related fields and 5 years of relevant experience. #J-18808-Ljbffr Charles River
Vacancy posted 4 days ago
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