刘家琳刘

Study Director – General Toxicology @ cro

About

I hold a PhD in Biomedical Sciences and currently work as a Study Director in GLP toxicology studies. I have extensive hands-on experience in animal models, toxicological evaluation, molecular biology, and biomedical research project management. I’m seeking career opportunities in the pharmaceutical or biotech industry, particularly in Medical Affairs, Regulatory Affairs, or Clinical Development roles, where I can bridge scientific insights with strategic execution. Based in Shanghai | Open to relocation | Fluent in Mandarin and English.

Country

China

City

Shanghai

Industry

Cosmetics

Skill

免疫荧光, 细胞培养, 实时荧光定量 PCR, 蛋白质免疫印迹分析法, image j, GraphPad Prism, Microsoft Excel, 数据分析, 学术研究, 应用研究, 研究项目, 研究

Experience

Study Director – General Toxicology

cro

2025-7 - Present · 1 yr 3 mos

• Responsible for designing, supervising, and reporting subchronic toxicity studies in compliance with GLP standards. • Coordinate cross-functional teams including pathologists, veterinarians, and lab technicians to ensure study integrity and timely delivery. • Conduct protocol writing, data review, and communication with sponsors. • Familiar with regulatory guidelines and toxicological endpoints (e.g., hematology, clinical chemistry, histopathology). • Manage study documentation and participate in QA audits and regulatory inspections. • Developed strong skills in project management, scientific writing, and interdepartmental coordination.