长沙招聘

？Responsibility：

     Assist the team in the preparation, handling, distribution, filing and archiving of documentation according to the scope of work and standard operating procedures.
？ Review documents for completeness, consistency and accuracy, under guidance of senior staff.
？ Prepare client deliverable documents using appropriate tools and may draft text for straightforward documents, under guidance of senior staff.
？ Assist with completion of relevant databases, tracking tools, timelines and project plans with project specific information.
？ Provide support for administrative tasks, e.g. meeting coordination, minute taking, travel arrangements, faxing, copying, couriers.
？ Interact with internal and external clients, under guidance of senior staff.
？ Perform IP release activities on projects or support reviews for larger projects. 

Qualifications：

？ A bachelor degree (or above) in a life science field. Proficiency in both written and spoken English.
？ Good interpersonal communication and organizational skills.
？ Good word processing skills and knowledge of MS Office applications. 
？ General awareness clinical trial environment and drug development process.
？ Ability to work on multiple projects.
？ Ability to establish and maintain effective working relationships with co-workers, managers and sponsors.

昆翎（ClinChoice）是一家致力于为生物医药和医疗器械客户提供高品质一站式服务的临床阶段CRO，服务包括临床运营、项目管理、生物统计、数据管理、注册事务、医学事务和药物警戒。昆翎已经在中国、美国、欧洲、印度、日本和菲律宾建立了主要的临床交付中心，目前在全球拥有1800多名员工，其临床运营团队覆盖了亚、欧、北美等七个国家和地区。

高盛直投部董事总经理、昆翎董事会成员许小鸥先生认为，“随着创新疗法在全球的增长，CRO公司提供高效、可靠的研发服务能力变得尤其重要。昆翎独特的价值主张结合了其对于本地市场的了解、国际药物研发的经验以及高效的团队执行能力。我们坚信公司强劲的管理层团队以及其高效的执行能力，将为昆翎的发展开启新的篇章。

昆翎是一家全球化的临床合同研究组织 (“CRO”)，在亚洲、北美洲和欧洲七个不同国家和地区拥有超过1800名临床研究专业人员。在全新品牌战略的引领下，昆翎将以“立足中国，服务全球”为己任，继续为全球制药、生物科技和医疗器械公司提供高质量、全方位服务的临床研究服务