工作职责:
? Organisation/Coordination of Regulatory Affairs related meetings/ events
组织协调注册事务相关的会议和活动
? Contribute to company activities/systems, support RA team to develop or enhance regulatory related SOPs, management systems, working procedures, etc. to improve team operational efficiency.
支持公司的活动和系统建设,支持RA相关流程的建立和改进
? Support department expenditures
支持部门费用的支出和报销
? Support interactions with cross-functions and external parties
支持跨部门和外部沟通联络
? Support the preparation of documents or tangible project materials
协助部门相关注册文件的准备
? Provide confidential administrative support to RA SVP
为RA SVP提供行政支持
? Fulfill any other tasks assigned by supervisor per business needs.
负责完成上级主管根据业务需求临时分派的其他工作任务
任职资格:
– Bachelor Degree or above,medical and pharmaceutical related science are preferred
本科及以上学历,医学和药学相关专业优先
– Fluency in Chinese, excellent English language verbal and written skills
流利的中英文口语和写作能力
– Good organizational and coordination skills are mandatory
良好的沟通协调能力
– Strong computer skills (MS Word, Excel, PowerPoint and Lotus Notes)
熟练计算机能力
– Positive appearance and good manners, assertiveness, flexibility
积极乐观,自信,有一定的灵活性
职能类别: 药品注册
关键字: 药品 注册
联系方式
上班地址:朝阳区
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