CTA - 临床项目助理 北京

月薪： 6-8千/月

该公司所有职位
  • 1年经验
  • 大专
  • 招若干人
  • 02-23 发布
  • 五险一金
  • 补充医疗保险
  • 交通补贴
  • 餐饮补贴
  • 专业培训
  • 年终奖金
  • 弹性工作
  • 定期体检

职位描述

PURPOSE OF THE JOB:?To assist the clinical research teams in ensuring the most effective and efficient conduct of clinical research studies by providing administration and project tracking support.JOB FUNCTIONS/RESPONSIBILITIES:?To provide general administrative support to the Clinical Operations Department and assistance to Project Manager(s) and Project Director(s).?To assist the Clinical Operations teams in completion of all required tasks to meet departmental and project goals.?To support the Clinical Operations teams with ongoing conduct of studies.?To be familiar with ICH GCP, appropriate regulations, relevant ICON SOP’s and ICON internal tracking systems.?To be familiar with the roles of the Clinical Research Associates (CRA) including site visits, if appropriate.?To assist project teams with study specific documentation and guidelines as appropriate.?To set up, organize and maintain clinical study documentation (e.g. Main Study Files, CRFs, etc.) including preparation for internal/external audits, final reconciliation and archival.?To process Data Collection Forms i.e. log in, tracking, quality control as appropriate for the study.?To assist in quality control audits of clinical study documentation (e.g. Main Study Files, CRF Files, Monitoring Files, etc.).?To co-ordinate ordering/dispatch and tracking of trial materials (e.g. CRFs, diary cards, lab supplies, drug supplies) as appropriate.?To assist project teams with trial progress tracking by updating the Clinical Trial Management systems.?To copy and route incoming correspondence, internal documentation, CRFs, etc., as appropriate.?To assist in co-ordination of Investigator payments, if applicable.?To contact clinical sites for specific requests (e.g., enrollment updates, missing documentation, meeting arrangements, etc.).?To assist in the tracking and distribution of safety reports.?To co-ordinate document translation, if required.?To attend project team meetings and generate meeting minutes.?To assist the Project Manager and project team with Investigator Meeting coordination, activities preparation and generate meeting minutes.?To assist in the production of slides, overheads, etc., as needed for project, departmental, sponsor and/or business development presentations.?To assist with the coordination of team member trackingQUALIFICATIONS/EXPERIENCE REQUIRED:?Either relevant work experience or High School Diploma (or equivalent).?Research or health care related academic or work experience preferable.?Good organizational skills, ability to manage multiple tasks and meticulous attention to detail.?Good written and verbal communication skills.?Good written and spoken English.?Computer literacy: e.g. Microsoft Word, Excel, PowerPoint, Outlook.?Willingness to travel for job related activities if required (expected travel for this position is < 10%) 职能类别： 临床研究员

联系方式

北三环东路36号环球贸易中心

公司信息

ICON Clinical Research-- a top global CRO company. For more details, please kindly see our website - http://www.iconplc.com/

北京相关职位

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北京相关职位： 分子生物学技术员 医药代表 市场专员 销售代表 政府事务经理(001055)(职位编号：gloria001055) 项目管理岗 食品相关产品注册客户服务主管 医疗器械注册及政策法规专员 临床项目经理 食品相关产品注册客户服务专员

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企业入驻日期： 2017-11-09

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