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职位描述
Provide support to study team as applicable. Responsible for completeness, quality, tracking, and accessibility of Central Files. Responsible for accuracy of coded documents/naming conventions for central files. Provide Clinical Lead and the team with detailed information on study procedures and study related materials. Ensure adherence to Good Clinical Practice, applicable regulatory and legal requirements as well as PAREXELs or clients SOPs. Responsible for up to date reports of study status in CTMS or client equivalent. Support Functional Leads in the set-up and maintenance of systems e.g. PMED. Organize project meetings and taking of minutes. Proactively flag and escalate any project related issues. Ensure CRF pages are being processed, tracked and forwarded to Data Management on time. Have up to date knowledge on study procedures and study related materials. Serve as a resource for the project team or Clinical team, depending on workload can be delegated to other project related tasks (e.g. set-up activities, other). Recommend process improvements for Clinical Research Assistant tasks. Contribute to the smooth running of the department and departmental activities e.g. arranging meetings and travel. Job Qualifications Skills Excellent interpersonal, verbal and written communication and customer service skills. Ability to communicate directly with study team members in an international environment. Ability to communicate directly with Sponsor / other vendors. A flexible attitude with respect to work assignments, new learning and travel. Demonstrated ability to manage multiple and varied tasks with positive attitude, prioritize workload with attention to detail and within agreed timescales. Willingness to work in a matrix environment and to value the importance of teamwork. Demonstrated ability to work independently and use initiative to complete tasks. IT literate – Experience with Microsoft based applications and general knowledge of PC functions, especially knowledge of Excel. Education Minimum education – high school diploma – ideally degree in life science, nursing qualification or other related background. Language Skills Competent in oral and written English and the local language. Minimum Work Experience Previous involvement as CRA assistant in an international study or similar experience in office management of international trial or other related experience would be preferred.
工作地点
上海 上海市 收起地图@2008-2023 大街网 京ICP备09028813号-1 人才服务许可证:1101052019005号 电子营业执照 京公网安备 11010802034037号 京ICP证090373号
北京大杰致远信息技术有限公司 公司地址:北京市海淀区成府路28号优盛大厦D座18层1801 联系邮箱:service@dajie.com 联系电话:4006371088(工作时间)