AD/Director, Toxicology

Role Overview

• Lead and own all in vitro and in vivo non-clinical toxicology activities (non-GLP & GLP) for multiple programs
• Design and communicate customized toxicology strategies for each program
• Attend program meetings, collaborate with cross-functional team leads, and guide project team leaders regarding toxicology and safety plans and timelines
• Plan, design, and oversee the execution of all outsourced CRO collaborations for toxicology and safety studies
• Manage, edit, and finalize collaborators’ (CRO) study reports
• Analyze, interpret, present, and communicate all preclinical toxicology and safety study findings
• Make key recommendations to project teams for mitigation strategies and next steps
• Author high-quality regulatory documents to support filings such as IND, CTA, NDA, and IB

Requirements

• Ph.D. in Toxicology, Pharmacology, Biology, or a related field; DABT preferred but not required
• 5+ years of professional experience in toxicology research or drug development in an industry setting; small molecule experience required
• Experience working with CROs in the US, Canada, EU, and Asia
• Professional level proficiency speaking English is required
• Professional level proficiency speaking Chinese is preferred

Benefits

• Competitive salary, benefits, and meaningful equity participation in a public company
• Annual bonus
• Stock-based long-term incentives
• Medical, dental, and vision benefits
• Retirement
• Wellness stipend
• Flexible time off