Description
Elevate patient care as a Lead Toxicology Expert at AbCellera. Bring your expertise in in vitro and in vivo toxicology to shape safe, effective medicines that make a difference.<br/><br/>In this senior role, you will oversee the design and execution of safety studies, ensuring compliance with global regulatory standards. You will act as a subject-matter expert in Nonclinical Safety, collaborating with cross-functional teams to drive project objectives. Your ability to analyze complex data and craft risk-benefit evaluations will guide executive decisions and ultimately enhance patient outcomes.<br/><br/>Key Responsibilities:
• Lead design and oversight of in vitro and in vivo studies
• Serve as SME for Nonclinical Safety in project teams
• Assess toxicology data and provide strategic recommendations
• Maintain comprehensive records in line with GLP standards
• Author and review regulatory documentation sections<br/><br/>Requirements:
• PhD in Toxicology or related field
• 5-8 years’ industry experience in biologics development
• Hands-on experience with toxicology studies
• Proficient in data analysis and communication
• DABT accreditation preferred but not required<br/><br/>Join AbCellera in driving breakthrough medicine development through expert toxicology assessment.
