Frontage Laboratories·Chicago, Illinois
The Study Coordinator supports non-clinical toxicology studies by generating protocols and amendments while coordinating study start meetings and client visits. They collaborate with Study Directors and other units to manage timelines and generate data tables using Provantis.
Title: Study Coordinator
Location: Chicago, IL (on-site)
Reports to: Director Laboratory Operations
Frontage Laboratories Inc. is an award winning, full-service, CRO/Contract Research Organization operating over 25 state-of-the-art laboratories across the US, Canada and China. Our core competencies include drug metabolism, pharmacokinetics/ pharmacodynamics (PK/PD), safety and toxicology, bioanalytical services, chemistry and manufacturing controls for drug development, and core laboratory services for clinical trials.
Our Chicago, IL site provides toxicology testing and research laboratory services and specialized pre-clinical studies in support of pharmaceutical and biotechnology products.
The individual in this position is involved in studies that evaluate the safety and/or toxicity of various materials (e.g., pharmaceuticals, chemicals, etc.). This position demands to be an active member of the study team and work along with the Study Directors and Report Writers and report to the Team Lead of Study Coordination group. This is a full-time on‑site position at our Chicago facility with no provisions for working remotely.
Roles and Responsibilities
Frontage Laboratories is seeking a highly motivated individual supporting Study Team for the non-clinical toxicology studies conducted under GLP regulations.
$21.64-26.45/hour, negotiable based on experience.
Frontage Laboratories Inc. is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex, sexual orientation, gender identity, age, status as a protected veteran, among other things, or status as a qualified individual with disability.
A Bachelor's degree in natural sciences is required, with a preference for experience in GLP and non-GLP toxicology studies. Candidates should possess strong scientific writing skills and familiarity with FDA, OECD, and GLP regulatory requirements.
Market context
In Illinois, Study Coordinator roles are typically tied to regulated research and lab operations, so demand often follows organizations running GLP and non-GLP toxicology work. These positions are competitive because employers look for a natural sciences degree, strong scientific writing, and familiarity with FDA, OECD, and GLP requirements. Review the AI-summarized requirements and benefits here to save research time, and tailor your application to show direct regulatory and study documentation experience.
