Senior Study Director, Toxicology – GLP & Regulatory Studies

Frontage Laboratories, Inc.

Chicago (IL)

Hybrid

USD 85,000 - 120,000

Full time

9 days ago

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Benefits offered by this job

401k Employer Match with immediatevest
Vision Insurance
Medical and Dental Insurance
FSA (Medical, Dependent Care, and Coms
Short Term Disability
Long Term Disability
Life Insurance
Generous Paid Holidays and PTO

Job summary

Frontage Laboratories Inc. in Chicago, IL is seeking a Study Director in Safety and Toxicology to lead nonclinical toxicology studies for regulatory submissions.

You will serve as the Study Director for Toxicology studies, including GLP studies, with overall responsibility for study conduct, data interpretation, and reporting. The role requires leading cross-disciplinary teams, ensuring GLP compliance, and delivering high-quality study results to clients.

Qualifications

  • PhD in toxicology or related field; DABT preferred but not required.
  • Experience across multiple disciplines and ability to manage multiple projects simultaneously.
  • Strong written and verbal communication skills; GLP regulatory knowledge; IACUC familiarity.

Responsibilities

  • Direct nonclinical toxicology studies as Study Director for regulatory submissions.
  • Oversee GLP toxicology studies (MTD/DRF, Acute, Sub-Chronic, and Chronic) and data interpretation.
  • Collaborate with management, staff, clients, and study-direction teams.

Skills

Leadership
Client interactions
GLP knowledge
IACUC familiarity
MS Office proficiency

Education

PhD in toxicology
Master's degree (2+ years relevant experience)
Bachelor of Science (5+ years relevant experience)

Tools

Microsoft Excel
Microsoft Word
PowerPoint

Job description

Frontage Laboratories Inc. in Chicago, IL is seeking a Study Director in Safety and Toxicology to lead nonclinical toxicology studies for regulatory submissions.

You will serve as the Study Director for Toxicology studies, including GLP studies, with overall responsibility for study conduct, data interpretation, and reporting. The role requires leading cross-disciplinary teams, ensuring GLP compliance, and delivering high-quality study results to clients.

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