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
Explicit and skilled 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
Solid knowledge of regulatory frameworks and compliance requirements

📌 Study Director / Technical Assistant Non Clinical Toxicity Studies Bengaluru
🏢 Eurofins
📍 Bengaluru