1、Be responsible for non-clinical pharmacokinetics studies of different molecular modality (small molecules, ADC, monoclonal antibodies, and polyclonal antibodies, etc.) at different stages (early screening, IND application evaluation, and clinical phase). 2、Responsible for the design, supervision, protocol, report review and data analysis of nonclinical toxicological studies for discovery and development projects. 3、Write M2.4, 2.6, IB and communicate with domestic and foreign regulatory authorities on non-clinical issues related to new drug application.