Office Secretary - Center for Clinical Research-临床研究中心办公室秘书-北京-01122

岗位职责
• Coordinate on SFDA & CFDA drug site application process
• Development an******** CCR office management system
• Coordinate IRB commun******** application process
• Coordinate clinical research relate********
• Refine an******** CCR relate********
• Coordinate with personnel relate******** CCR office
• Coordinate relevant meetings with different departments
• Atten******** trainings as required
• Other duties as assigned
任职条件
• Holder of Bachelor's Degree or Mater's Degree in Bio-chem,Chem******** Pharmacy, Laboratory, Me******** Nurse or other relevantmajors
• Previous research or clinical experience; familiar with policiesan******** relate******** the clinical research
• Familiar with medical terminology an******** in working in medicalsetting on day-to-day basis
• Ability to comply with regulate********, policies an********; able toorganize an******** tasks
• Effective oral an******** communication skills in English an********
• Skill in exercising ******** ju******** problem solving.
• Professional telephone etiquette
• Self-mot******** strong organizational sk******** an********initiative to work independently to meet deadlines
职位概述
Summary of Responsibilitie********
Will play an important role in assisting with the continue******** ofCenter for Clinical Research an******** Review Board, including the CFDAdrug site application process an******** communication an******** of theoffice
部门概述
CENTER FOR CLINICAL RESEARCH

Mission Statements
The Center for Clinical Research (CCR) of the Unite******** Healthcare(UFH) promotes an******** clinical research conducte******** all the UFHfacilities. Clinical research means any systematic investigation thatinvolves human subjects.

The UFH Center for Clinical Research promotes an******** ******** at allthe UFH sites in Ch******** to ******** conduct an******** of clinicalresearch projects. These projects may ******** but not limite********,case reports, retrospective analys******** clinical trials of drugsan********, an******** studies. These projects may be UFHinvestigator-initiate********, collaborate******** with other ********or studies sponsore******** private companies or governmental agencies.