Global Business Development Direrctor -South America

Responsibility Summary ：①Lead the team to draft the multi regional clinical trial protocol; ②supervisor of medical monitor on the clinical trials of new entities; ③and medical communication with the registration departments. 1 - Clinical R & D Strategy - Assist in clinical R&D strategies of new drugs; Participate in make clinical R&D strategies and indications of new entities at company-level and evaluation of clinical development; 2 - Clinical Trial Protocol - Responsible for guiding and reviewing the clinical trial protocol，Provide guidance and suggestions for team members to prepare clinical trial protocols; -Revise and review the clinical trial protocol prepared by each medical manager. 3- Implementation of clinical medicine monitor - Guide team members and review team members work Including: monitoring plan,training materials - Cross-function communication & problem solving - Medical support Cooperate with other departments to provide medical professional advice; Review subordinates' work about the medical registration application materials. Qualification -Education:Master degree or above, prefer doctor major in medicine or relative. -Work Experience:At least 8 years of working experience in clinical or pharmaceutical enterprises.Familiar with global new drug development process and clinical trial from Phase-I to Phase-III with experience in clinical monitoring and protocol draft. -Skills ①English skills：Good English reading writing and speaking, literature searching and translation skills. Ability to write medical documents and communicate with different drug authorities. ②Computer skills: familiar with office software- word / excel / ppt