Assist physician for China development strategy and plan (includingprotocols) for all portfolio projects.
Assist physician to ensure successful conduct and integrity of allin-scope clinical studies (i.e., providing medical monitoring).
Assist physician to co-own of clinical study delivery (with Stats andClinical Operations).
Assist physician for development clinical documents (CIB, protocol andCSR, etc.).
Assist physician to analysis and interpretation of clinical studyresults in partnership with Biometrics.
Assist physician to forming and running advisory board for portfolio projects.
Support protocol development preparation for review by the ClinicalChallenge and Protocol Review Committee.
Supporting China regulatory filing and registration.
Ph.D or M.D degree of clinical, biomedical, scientific
General therapeutic area/disease Knowledge
General compound knowledge
General Regulatory knowledge
Investigator & site knowledge
Basic Medical monitoring
Safety monitoring and evaluation of signals
CSP/CSR content & data analysis
Presentation & communication skill