Study Director / Technical Assistant - Non-clinical Toxicity studies

2.0 KEY RESPONSIBILITIES 2.1 Study Leadership and Regulatory Compliance 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 Demonstrate expertise in GLP-compliant non-clinical toxicity study design and execution Administer test items via multiple routes of exposure with proficiency and precision 2.2 Data Management and Scientific Reporting Conduct thorough review of study data to identify deviations and inconsistencies Evaluate study results objectively and prepare high-quality study reports, amendments,…