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1. Develop product clinical development strategy and implementation plan under the coaching of superiors and the supervision of appropriate departments.
2. Under the guidance of superiors, skilled in organizing and writing materials related to medical clinical trials of CDE communication meetings.
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. 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).
6. Serve as primary technical contact with client under the guidance of superiors and appropriate departmental supervision.
Special Requirement"
1. Have a certain degree of market sensitivity and insight into the pharmaceutical industry.
2. Have certain abilities in researching and summarizing customer and product development situations."
1. Master or Ph.D major in medical science or life science.
2. Be able to learn quickly and master the key points of clinical trials and relevant policies and regulations.
3. Languages: Excellent written and read English. Excellent oral English are preferred.