1. Responsible for the preclinical pharmacodynamics of the company's new drug development Organize relevant data on toxicology and pharmacokinetics, develop pharmacological and toxicological development plans for new drug research and development, and participate in animal experiments at the animal center;
2. Responsible for CRO research to examine. Administration. Implement relevant research, track experimental progress, and analyze and summarize experimental results;
3. Responsible for researching the plan Review of technical materials such as summary reports;
4. Responsible for translating the pharmacological and toxicological sections of new drug approval documents Writing and registering CMC collaborates with clinical personnel to complete the work related to new drug application;
1. Bachelor's degree or above in pharmacology Background in toxicology and related fields,
2. Familiar with the requirements of national technical review and relevant regulations of national drug administration (NMPA&FDA) and ICH guiding principles;
3. Ability to translate English literature and Chinese reports