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.