1、Be responsible for searching domestic and foreign literatures and information, and timely tracking, collecting and organizing domestic and foreign information and data about diseases and new drug development interested by the company;
2、Be responsible for preparing and reviewing documents related to clinical trials, such as clinical research report, clinical trial scheme, investigator’s brochure, informed consent, and clinically relevant part of IND/NDA declaration materials;
3、负责医学相关支持计划（例如，医学监察计划、）的实施Be responsible for the implementation of medical support program (such as medical surveillance program)；
4、Be responsible for inner and external medical trainings;
5、Be responsible for medical inspection and data verification in the process of clinical trial;
6、Assist clinical operation team, and communicate and coordinate with researchers;
7、Tackle other tasks assigned by direct supervisor.。

1、Master of clinical medicine, traditional Chinese medicine, pharmacy, and other related fields or above;
2、With over 1 year of work experience related to clinical medicine;
3、With at least 1 year of work experience of drug research and development or clinical study, and familiar with whole process of clinical study of Phase I, II or III, and ICH-GCP and Chinese GCP provisions;
4、Good writing skills, communication skills, organizational coordination ability, and team-work spirit;
5、Strong sense of responsibility, ability to work under pressure, and initiative and proactivity.