Responsibilities 工作职责
a) Be responsible for archiving the related regulatory documents and corresponding electronic files.
负责项目相关文件的存档管理，包括纸版文件和电子版文件：20%
b) Be responsible for the translation, proofreading, and printing, copying, and shipping of the registration
dossier and so on.
负责注册文件的翻译，校对，打印，复印，装订，运输等：20%
c) Be responsible for daily admin work in RA department，including answering the telephone call，
arranging meeting or conference, monthly reimbursement, man-hours records and so on.
负责部门日常行政支持工作，包括电话接听，会议安排，费用报销，人工工时统计等： 20%
d) Be responsible for archiving of contracts of RA projects, preparing for the invoice, payment checking
with project leader and Financial Department, etc.
负责注册相关项目合同的存档，项目发票的准备，和项目负责人及财务部核对收款等；20%
e) Be responsible for the archiving of SOP files, updating of the staff CV in RA department and so on;
负责SOP 文件存档，部门员工CV 的整理和存档等：10%
f) Others 公司交付的其他工作：10%
Minimum Qualifications 最低任职资格

a) Academic / Major 学历/专业:
Bachelor degree or plus，major in Medical, Pharmacology, Biology and related specialties.
本科以上学历，医学，药学，生物学或相关专业。
b) Professional Skills 专业技能要求:
Good at paper work, and knowledge to local regulations is preferred.
擅长文案工作，了解注册相关法规优先。
c) Language ability 语言能力:
Fluent in both written and spoken Chinese; Fluent in both written and spoken English.
中英文说写流利。
d) Computer Literacy 电脑相关知识:
Good command of Microsoft offices.熟练使用常用办公软件。
e) Others 其它:
Strong communication skill is preferred; 较强的人际交往能力。