GLP Toxicology Study Director – Senior Scientist

AbbVie; North Chicago (IL); On-site; USD 120,000 - 180,000; Full time

Job summary

AbbVie seeks a GLP Study Director to lead internally conducted toxicology studies (80%) and to monitor external sponsor studies at contract research organizations. You will ensure the highest standards of GLP quality and regulatory compliance in study conduct and reporting.

You will serve as the scientific expert during audits and contribute to filing documents for global regulatory submissions, communicating key findings effectively to teams and leadership.

Qualifications

• Experience as GLP study director in toxicology.
• Strong regulatory reporting and quality standards.
• Ability to communicate complex findings clearly.

Responsibilities

• As study director, ensures GLP quality and regulatory compliance in study conduct and reporting.
• Accounts for GLP report authorship, writing and reviewing toxicology study reports and filing components.
• Represents sponsor in audits, project teams and regulatory submissions.

Skills

GLP compliance

Toxicology

Regulatory reporting

Scientific writing

Project management

Job description

AbbVie seeks a GLP Study Director to lead internally conducted toxicology studies (80%) and to monitor external sponsor studies at contract research organizations. You will ensure the highest standards of GLP quality and regulatory compliance in study conduct and reporting.

You will serve as the scientific expert during audits and contribute to filing documents for global regulatory submissions, communicating key findings effectively to teams and leadership.