昆翎医药欢迎最新从事过临床监查员等行业的优秀人才加入我们，昆翎企业管理（上海）有限公司将为您提供广阔的发展平台！
工作职责：
1.Assist the team in the preparation, handling, distribution, filing and archiving of documentation according to the scope of work and standard operating procedures.
2.Review documents for completeness, consistency and accuracy, under guidance of senior staff.
3.Prepare client deliverable documents using appropriate tools and may draft text for straightforward documents, under guidance of senior staff.
4.Assist with completion of relevant databases, tracking tools, timelines and project plans with project specific information.
5.Provide support for administrative tasks, e.g. meeting coordination, minute taking, travel arrangements, faxing, copying, couriers.
6. Interact with internal and external clients, under guidance of senior staff.
7.Perform IP release activities on projects or support reviews for larger projects.
任职资格：
1.A bachelor degree (or above) in a life science field. Proficiency in both written and spoken English.
2.Good interpersonal communication and organizational skills.
3.Good word processing skills and knowledge of MS Office applications.
4.General awareness clinical trial environment and drug development process.
5.Ability to work on multiple projects.
6.Ability to establish and maintain effective working relationships with co-workers, managers and sponsors.
