GLP Study Director, Toxicology - Senior Scientist

Allergan; Chicago, Northern (IL, KY); Hybrid; USD 120,000 - 180,000; Full time

Benefits offered by this job

Health insurance

401(k) plan

Paid time off

Job summary

AbbVie in Illinois seeks a Toxicology Study Director to lead GLP toxicology studies and oversee external CRO monitoring. The role centers on ensuring regulatory compliance, accurate report writing, and timely support for submissions in development.

The position requires a PhD in Toxicology (or related field) and strong communication skills, with responsibility for study design, data interpretation, and cross-functional collaboration within a fast-paced team.

Qualifications

• PhD in Toxicology or closely related field.
• Experience with GLP-compliant toxicology studies is required.
• Excellent written and verbal communication for regulatory submissions.

Responsibilities

• Serve as GLP Study Director for internally conducted toxicology studies (80%) and monitor CRO studies (≤20%).
• Ensure quality and regulatory compliance in study conduct and reporting.
• Author GLP study reports and contribute to filing documents for regulatory submissions.
• Manage study timelines and coordinate with line management to meet regulatory needs.

Skills

GLP compliance

Toxicology

Study director

Regulatory communication

Report writing

Education

PhD in Toxicology or related field

Post-doctoral training (optional)

Job description

AbbVie in Illinois seeks a Toxicology Study Director to lead GLP toxicology studies and oversee external CRO monitoring. The role centers on ensuring regulatory compliance, accurate report writing, and timely support for submissions in development.

The position requires a PhD in Toxicology (or related field) and strong communication skills, with responsibility for study design, data interpretation, and cross-functional collaboration within a fast-paced team.