Study Director / Technical Assistant - Non-clinical Toxicity studies

About the role

2.1 Study Leadership and Regulatory Compliance Demonstrate expertise in GLP-compliant non-clinical toxicity study design and execution 2.3 Cross-Functional Coordination and Stakeholder Management Scientific and analytical thinking with strong problem-solving capabilities Meticulous attention to detail with commitment to quality excellence

What you'll do

• Serve as Study Director, Principal Investigator, or Technical Assistant for non-clinical toxicity studies
• Ensure full compliance with GLP, OECD, ICH, FDA, and EPA guidelines, as well as sponsor-specific requirements
• Lead all aspects of study execution, including planning, conduct, oversight, data interpretation, and comprehensive reporting
• Administer test items via multiple routes of exposure with proficiency and precision
• Conduct thorough review of study data to identify deviations and inconsistencies

What you need

• GLP
• Documentation
• Communication
• Any graduate