Study Director / Technical Assistant - Non-clinical Toxicity studies
BengaluruFull-timeLead levelPosted 4 days ago
Leadership pharma role at Eurofins in Bengaluru.
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