Principal Research Associate/ Toxicology Study Coordinator

This position is responsible for planning, coordinating, and overseeing nonclinical toxicology studies supporting discovery, IND-enabling, and post-marketing programs. The individual will ensure that studies are conducted with appropriate quality, GLP compliance, scientific rigor, and alignment with program timelines.

Responsibilities

also include reviewing, organizing, and summarizing study data, and providing study updates to project teams and other internal stakeholders. This position reports to the Vice President of Toxicology and works closely with toxicologists and the Toxicology Operations team to coordinate study activities, support data review, and address departmental operational priorities.

This is a full-time, on-site position based in Carlsbad, CA.