Medical (Clinical Research) Post

1. Responsible for the specific implementation and execution of clinical research for ongoing projects

2. Assist in carrying out various tasks related to clinical trials to ensure their smooth progress

3. Responsible for writing clinical trial related materials for ongoing projects (including IND application medical materials and ethical materials, etc.);

4. Responsible for communicating important project related matters with clinical CROs and researchers;

5. Responsible for clinical efficacy and safety data analysis, and can provide support for the subsequent development strategy of the project;

6. Responsible for reviewing the clinical trial summary report, reviewing the data during the clinical trial process, raising medical questions, and proposing solutions.

1. Clinical medicine related majors, master's degree or above, with clinical experience or pharmaceutical company medical department workers preferred;

More than 2.5 years of work experience in the same position, excellent candidates can be relaxed;

3. Familiar with the entire process of clinical research and the requirements of relevant regulations for clinical trial management, with experience in IND application and writing Phase I-III clinical related materials;

4. Strong communication skills, language expression ability, teamwork and cross departmental collaboration ability, able to adapt to part-time business trips.