Senior Scientist, Study Toxicologist

As a pivotal member of the Nonclinical Safety team, the Senior Scientist, Study Toxicologist, reporting to the Associate Director, Toxicology Study Operations, will play a critical role in collaborating with project toxicologist and managing the outsourcing, design, and oversight of safety pharmacology and toxicology studies at contract research organizations (CROs). Additional responsibilities include collaborating with toxicology project leads, serving as the primary sponsor representative for CROs, overseeing the design and execution of nonclinical safety studies, reviewing study reports and SEND datasets, communicating study findings, contributing to regulatory submission documents, and developing departmental SOPs. The ideal candidate will have a PhD with 5+ years, MS with 8+ years, or BS with 12+ years of experience as a study director/monitor in toxicology. They will also possess advanced knowledge of toxicology, in-depth understanding of GLP regulations, enthusiasm for scientific research and strong critical thinking skills.