Typical Accountabilities:

Works closely with lead physician of a study, project or compound to take medical responsibilities to ensure successful

conduct and integrity of all in-scope clinical studies.

• Develops clinical development knowledge/skills and good understanding of GCP and maintains up-to-date

medical/scientific knowledge in the TA.

• Provides medical expertise to support medical feasibility to study protocol, and assists site feasibility and selection

when necessary.

• Under supervision of study lead physicians to support medical monitoring for the trials to review medical data,

evaluate AEs/SAEs and find out issues, to ensure the data with high quality and the safety of participants.

• Supports document preparations for EC submission, China regulatory filing and registration as a TA clinical science

expert.

• Provides scientific training on disease knowledge, product and protocol to cross-functional team members and external

patterners as clinical science physician.

• Keeps close connection with global study team during the entire course of the study.

• Builds up network with KOLs in the TA and seeks their opinions for clinical and research projects as needed.

• Other tasks assigned by line manager as appropriate

Qualifications:

• M.D. degree or Ph.D. in scientific discipline

• Extensive general medical knowledge

• Experience in clinical research