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 project teams to ensure high-quality regulatory data delivery for drug development and marketing authorisation. This position requires expertise in regulatory toxicology, study design, and cross-functional communication to mitigate safety risks across various therapeutic modalities.