Teams at Frontage Laboratories, Inc

Prepares, formats, reviews, and finalizes preclinical toxicology reports, protocols, and related sponsor-facing documents. The role compiles and summarizes study data, manages tables and templates, performs quality checks, coordinates information from study teams and subcontractors, tracks report progress, and resolves production issues. It requires adherence to regulatory, SOP, protocol, and sponsor guidelines while maintaining accurate documentation and meeting deadlines.

The role involves overseeing toxicology studies, managing a team of scientists, ensuring compliance with regulations, and engaging with clients.