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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.
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Worksite address
north chicago, IL, 60086, US
Who can apply
Review the original listing for work authorization, qualifications and employer requirements.