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********.