Study Coordinator

Title: Study Coordinator

Location: Chicago, IL (on-site)

Reports to: Director Laboratory Operations

Full-time

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.

Position/Job Summary

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.

Key Responsibilities

Generation of study protocol based on the signed study proposal

Generation of protocol amendments, if and when needed

Scheduling and conducting the study start meetings

Coordinate client visits, when requested by the client

Generating data tables from Provantis

Collaborate with other units to support study timelines

Interact with Study Directors and help define study priorities and schedules