Responsibilities: pay attention to the updating of current laws and regulations, build and perfect the ADRM system which can meet the reqirements of laws and regulations; collect, analyze, evaluate and report ADRs; check the ADR information regularly and make an analyzed report; summit annual ADR report; participate the evaluation of safety risk and benefits; promote and check the safety updating report reguarly; organize and coordinate related departments to evaluate, investigate and report the SAEs and cooperate the checking from durg monitoring, health administration and ADRM authorities; sopport other departments on drug safety; participate the training organized by ADRM authorities; organize and promote the ADRM training.
Qualificaiton：fulltime bachelor or above degree; biology, medicine and Veterinary medicine; Have junior professional title certificate or licensed pharmacist certificate and experience in pharmaceutical industry is preferred; be familiar with GMP, have the experience of ADR and phamaceutical firms management is preferred; can express ideas orally fluently and good communication ability; be careful and positive and innovative; be familiar with office software; have the ability in writing and organization.
Welfare:
social insurance and housing bonus; perfect attendance bonus; 8-hour work; holiday welfare; free working meal; physical examination.