Position Summary Closely working with medical writers an******** physicians to contributeto clinical study relate******** writing activities to meet customer’sclinical trial project needs. He / she will carry out day-to-dayhands-on work an******** goo******** writing relationships with projectrelate******** internally an********.
Key Responsibilities - To work directly with medical writing manager, clinicalphys********b******** programmers, or relevant parties involve********all medical writing activities. - To carry out hands-on medical writing in accordance with company SOPs an********. - To participate in the discussion an******** the clinical developmentplan an******** - To prioritize an******** workloa******** a high standard - To work directly with medical team an******** research physician tocarry out clinical study relate******** writing including IB, studysynops******** protocol, CSR, clinical document translation. - To search pro******** target indication with market analysis an******** - To be involve******** the preparations on the documentation forregulatory submissions (e.g. investigator brochures, protocols, an********). - Develop an******** sol******** of the relevant therapeutic areasan******** writing techniques. - To undertake any activities involving writing an******** with others,internally an********, as requested.
Professional Experience & Education Requirement - Bachelor degree in Me******** pharmacology or other life sciencedegrees (or equivalent) - Understan******** trial operation process - Excellent Chinese an******** written an******** communicationskills;excellent scientific an******** writing skills in both Chinese an********.