Research Assistant

Supported preclinical research studies by maintaining test materials, documentation, and ensuring compliance with OECD GLP standards. Collaborated with multidisciplinary teams including pharmacologists, toxicologists, and veterinarians to facilitate preclinical study execution.

Key Contributions & Impact

• Test Materials and Documentation Management: Maintained test materials and documentation for preclinical studies in compliance with OECD GLP standards.

• Interdisciplinary Collaboration: Collaborated with pharmacologists, toxicologists, and veterinarians on preclinical studies, ensuring proper study execution and regulatory compliance.

Technologies Used

OECD GLP Standards, Preclinical Research, Documentation Management, Regulatory Compliance