Study Monitor

A Study Monitor at AstraZeneca's Safety Sciences China group supports the design, conduct, and reporting of non-clinical in vivo toxicology studies at Contract Research Organisations (CROs). The role involves collaborating with global colleagues and internal stakeholders to ensure high-quality toxicological data is delivered for clinical studies and regulatory submissions. This position requires an experienced in vivo toxicologist to oversee study execution and provide expert scientific input across various therapeutic areas and modalities.