该职位来源于猎聘

Develop product clinical development strategy and implementation plan under the coaching of superiors and the supervision of appropriate departments.
Under the guidance of superiors, skilled in organizing and writing materials related to medical clinical trials of CDE communication meetings.
Establish good communication relationship with medical experts in key fields, and close communication about research programs.
Draft, review, and QC of clinical documents to ensure compliance of documentation to GCP, SOPs.
Work closely with CO, RA, BD, PV and other departments, provide advice, support and assistance according to project needs (select of

PI/Participate in project meetings and protocol discussion).

Serve as primary technical contact with client under the guidance of superiors and appropriate departmental supervision.
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.
Master degree major in medical science, More than 1 years clinical experience in oncology or chronic disease therapeutic area.
Or bachelor degree in medicine, More than 5 years clinical experience in oncology or chronic disease therapeutic area, and more than 2 years MA experience.
Be able to learn quickly and master the key points of clinical trials and relevant policies and regulations.
Languages: Excellent written and read English. Excellent oral English are preferred.