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, and responses to sponsor inquiries - Ensure timely and accurate submission of all scientific documentation  2.3 Cross-Functional Coordination and Stakeholder Management   - Coordinate effectively with sponsors, pathology, analytical, bioanalytical, veterinary, and quality assurance teams - Maintain adherence to study timelines and deliverables - Participate in sponsor meetings and provide regular study updates - Support regulatory submission activities  2.4 Core Competencies   - Scientific and analytical thinking with strong problem-solving capabilities - Meticulous attention to detail with commitment to quality excellence - Sound decision-making and critical thinking skills - Clear and professional communication with sponsors and cross-functional teams - Leadership capability with mentoring potential - Full accountability and ownership of study deliverables - Excellent time management and ability to meet strict deadlines - Strong knowledge of regulatory frameworks and compliance requirements