Experience

AffaMed Therapeutics

• China
• Biotechnology
• 1 - 100 Employee

• Assistant director

  • Nov 2020 - Present

  Clinical research physician Clinical research physician



Shanghai Haohai Biological Technology Co.,Ltd.

• Shanghai City, China

• Assistant Department Manager

  • Jun 2017 - Nov 2020

  1. Provide professional suggestion and academic support to eye care products. 2. Implement academic surveys in ophthalmology area and report to leadership termly. 3. Evaluate the world-wide creative projects in ophthalmology and write assessment report. 4. For a project with a research partnership, I need to implement elementary evaluation, confirm the cooperation model and financial budget, make a research plan and build a research team for the project. 5. Write the protocol and CRF of pro-market and post-market clinical trial for eye care products, and carry out the clinical trial project management. 6. Manage medical department.



Allergan

• Shanghai City, China

• Medical Manager

  • Jun 2010 - Jun 2017

  1. Take the responsibility for Medical Strategy and medical projects management for tears and steroid products and dry eye pipelines. 2. Provide medical insight to business partner, co- lead with business partner for brand plan and strategy. 3. Identify and develop professional relationships with key KOLs in China 4. Provide internal and external training to MSL, commercial team and HCPs regarding optimal use of Allergan’s products with regards to anatomy, product knowledge, and methodologies for assessing patient outcomes. 5. Take responsibility of tears and steroid products and dry eye pipelines’ Phase IV, IIT studies management. 6. 6. Article writing and publishing.



InCROM

• Shanghai City, China

• Project Manager

  • Jul 2009 - Jun 2010

  1. Design protocol, CRFs and communicate with sponsors. 2. Initiate, monitor and close clinical trials in compliance with study protocol, GCP and SOP. 3. Control the progress of clinical project according to the timeline and financial budget. 4. Manage and resolve study related issues in the project progress. 1. Design protocol, CRFs and communicate with sponsors. 2. Initiate, monitor and close clinical trials in compliance with study protocol, GCP and SOP. 3. Control the progress of clinical project according to the timeline and financial budget. 4. Manage and resolve study related issues in the project progress.