Study Coordinator

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

If you are unable to complete this application due to a disability, contact this employer to ask for an accommodation or an alternative application process.

Full Time Chicago, IL, US

3 days ago Requisition ID: 1860

Salary Range: $21.64 To $26.45 Hourly

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

Qualifications and Experience

• 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.

Salary

• 401k Employer Match with immediate vesting
• Vision Insurance
• Medical and Dental Insurance with multiple coverage options
• FSA (Medical, Dependent Care, and Commuter)
• Short Term Disability
• Long Term Disability
• Life Insurance
• Generous Paid Holidays and PTO

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.