Primary Responsibilities:

1. Develop product clinical development strategy and executive plan

under appropriate departmental supervision.

2. Skilled in organizing and writing materials related to medical

clinical trials of CDE communication meetings, attending face-to-face

meetings and communicating with CDE experts when necessary.

3. Establish good communication relationship with medical experts in

key fields, and close communication about research programs.

4. Draft, review, and QC of clinical documents to ensure compliance of

documentation to GCP, SOPs.

5. Development medical supervision plan and function as a medical

monitor in case of need, to ensure the quality and safety of the project,

including but not limited to the monitoring of SAE and programme deviation.

6. Work closely with CO, RA, BD, PV and other departments, provide

advice, support and assistance according to project needs (select of leading

PI/ Participate in project meetings and protocol discussion).

7. Serve as primary technical contact with client under appropriate

departmental supervision.

8. Provide medical professional guidance to subordinates.

Qualification：

1. Ph.D. in Medical Science, More than 1 years clinical experience in

oncology or chronic disease therapeutic area.

2. Or master degree major in medical science, More than 3 years

clinical experience in oncology or chronic disease therapeutic area.

3. Or bachelor degree in medicine, More than 5 years clinical

experience in oncology or chronic disease therapeutic area.

4. Be familiar with the key points of clinical trials and relevant

policies and regulations.

5. Languages: Excellent written and read English Excellent oral

English are preferred.