Associate Director, Study Operations Manager - Nonclinical Toxicology

The Associate Director, Study Operations Manager - Nonclinical Toxicology oversees the end-to-end operational management of nonclinical toxicology and safety pharmacology studies conducted by external CROs. This role ensures scientific quality, regulatory compliance, and alignment with study objectives while managing data flow and coordinating with internal and external teams. The position involves monitoring study progress, tracking key milestones, and supporting the advancement of preclinical candidates to inform scientific decisions and development milestones.