Lead non-clinical safety efforts at AbCellera as a Principal Scientist focused on innovative drug development. Oversee toxicological studies while ensuring compliance with regulatory standards in Vancouver, Canada.

As a key member of the non-clinical safety team, you will design and implement toxicology programs supporting drug applications and clinical trials. This full time role involves collaborating with contract research organizations and providing strategic oversight for protocol development and study execution. Your insights will guide candidate selection, risk assessment, and aid in regulatory documentation process.

Key Responsibilities:
• Lead toxicological studies for drug applications
• Collaborate with contract research organizations




• Guide cross-functional program teams on toxicology
• Communicate risk-benefit assessments to management
• Develop non-clinical safety strategies across products

Requirements:
• Expertise in non-clinical toxicology and regulations
• Proven experience supervising toxicological studies
• Ph.D. in toxicology or related field with 8+ years' experience
• Strong writing skills for regulatory documents
• Ability to manage multiple projects simultaneously

Utilize your expertise in toxicology to significantly impact drug development at AbCellera.
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📌 Principal Scientist Non-Clinical Safety (British Columbia)
🏢 AbCellera
📍 British Columbia