Senior Toxicology Study Director (GLP)

BioSpace; North Chicago (IL); On-site; USD 120,000 - 170,000; Full time

Benefits offered by this job

Paid time off

Medical/dental/vision insurance

401(k)

Job summary

AbbVie is seeking a GLP Study Director in toxicology to lead internally conducted studies and monitor external sponsor work. The role emphasizes high standards of quality, regulatory compliance, and timely reporting for regulatory submissions.

The incumbent will author GLP reports, communicate findings, manage timelines, and contribute as a scientific expert in audits and project teams, with potential progression to Sr Sci I/II based on experience.

Qualifications

• GLP and non-GLP study conduct and project science within Toxicology.
• Ability to design/interpret experiments, record and report results.
• Communicate findings in reports and meetings.

Responsibilities

• Serve as GLP Study Director for internal toxicology studies (80% time) and external sponsor monitor.
• Ensure quality and regulatory compliance in study conduct and reporting.
• Manage study timelines aligned with regulatory filing needs and project plans.

Skills

Toxicology expertise

GLP compliance

Regulatory knowledge

Strong communication

Study design & analysis

Education

PhD in Toxicology

Master's in Toxicology

Bachelor's degree in related field

Job description

AbbVie is seeking a GLP Study Director in toxicology to lead internally conducted studies and monitor external sponsor work. The role emphasizes high standards of quality, regulatory compliance, and timely reporting for regulatory submissions.

The incumbent will author GLP reports, communicate findings, manage timelines, and contribute as a scientific expert in audits and project teams, with potential progression to Sr Sci I/II based on experience.