Descripion

Comply with relevant GLP regulations, assist the project leader in participating in toxicology and pharmacological safety evaluation tests, complete quality control of the entire experiment, analyze experimental data, and collect and organize records; Assist the project leader in writing the report.

Requirement

1. Education: Master's degree
2. Major: Pharmacology, Toxicology related majors;
3. Other: Experience in project management for non clinical research CRO companies; Familiar with the design of drug efficacy and toxicity test plans, able to correctly interpret data; Understand the requirements of regulations and guidelines related to non clinical animal trials in new drug applications; English proficiency level 6 or above, able to access medical English literature; Priority will be given to those who meet the above conditions.
Job benefits: weekends off; Pay the five social insurances and one housing fund; Work lunch; Annual health check ups; Internal and external professional training and academic exchange activities.