Toxicology Study Coordinator — On‑Site in Chicago (GLP)

Frontage Laboratories, Inc.; Chicago (IL); On-site; USD 29,811 - 36,437; Full time

Benefits offered by this job

401k Employer Match

Vision Insurance

Medical and Dental Insurance

FSA (Medical, Dependent Care, and Com/

Short Term Disability

Long Term Disability

Life Insurance

Paid Holidays and PTO

Job summary

Frontage Laboratories Inc. in Chicago, IL is seeking a dedicated professional to support non-clinical toxicology studies under GLP regulations.

This on-site, full-time role works with Study Directors and Study Coordination to ensure study timelines and data quality. The ideal candidate holds a BS or equivalent in natural sciences, has experience with GLP/non-GLP toxicology, strong scientific writing, and familiarity with FDA/OECD guidelines.

Qualifications

• BS or equivalent in natural sciences.
• Experience supporting Non‑GLP and GLP non‑clinical toxicology studies is preferred.
• Excellent scientific writing and documentation skills.
• Ability to work independently and in a fast‑paced CRO environment.
• Familiarity with FDA, OECD, and GLP regulatory requirements is preferred.

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.
• Demonstrates the ability to contribute to the success of assignments.
• Performs other duties as assigned.

Skills

Scientific writing

Independent work

Regulatory familiarity

Education

BS or equivalent in natural sciences

Job description

Frontage Laboratories Inc. in Chicago, IL is seeking a dedicated professional to support non-clinical toxicology studies under GLP regulations.

This on-site, full-time role works with Study Directors and Study Coordination to ensure study timelines and data quality. The ideal candidate holds a BS or equivalent in natural sciences, has experience with GLP/non-GLP toxicology, strong scientific writing, and familiarity with FDA/OECD guidelines.