Responsibilities: 1) Administrative support; 2) Desk research to summarize some basic information of clinical trial related;  3) Coordinate with regional team on the China registered site information;  4) Maintain and update teams request tracker, external medical advisor list, internal study experience tracker, etc; 5) Work closely with legal team about the latest version of ICA(Contract), and document stamp/signature support; 6) Work closely with finance team on the payment application and status tracking. Requirements: Bachelor's Degree and above, Life sciences or other related field Skilled in use of  Microsoft Office (especially MS Excel skills, Python is a plus); Knowledge of clinical trial; Strong written and verbal communication skills including good command of English language;