Senior Scientist, Toxicology I

Role: GLP Study Director for AbbVie's toxicology studies, ensuring quality, regulatory compliance, and scientific integrity in both internal and external studies. Responsibilities: oversee study conduct, authorship of report documentation, and regulatory filing preparations; serve as scientific expert during audits and project discussions; manage timelines aligned with development milestones; apply regulatory standards (FDA, ICH, OECD) and scientific expertise to study design and interpretation. Requirements: PhD in Toxicology or related field with up to 4 years of study director experience; or Master’s/Bachelor’s with 8-10 years of relevant experience; strong knowledge of GLP, regulatory guidelines, and toxicology study practices; excellent communication and problem-solving skills. High-Value: toxicology (pharmaceutical), GLP compliance, report writing, regulatory filings, cross-functional collaboration. WorkSetup: not specified; designed for office-based or lab environment; no travel explicitly mentioned.