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无工作经验 -
本科 -
招1人 -
11-09 发布
- 五险一金
- 年终奖金
- 通讯补贴
- 公司午餐
- 专业培训
职位描述
职位描述： To provide administrative support of the set-up, tracking and reporting of clinical trials in conformity with Good Clinical Practice (GCP) and company Standard Operation Procedures (SOPs) in order to facilitate to a high extent the execution of the research projects;- Perform all duties/responsibilities in a professional manner;- Handle/record confidential corporate documents;- Screen incoming calls and all correspondence and respond independently when possible;- Maintain various tracking logs;- Maintains/updates board manuals and resource materials;- Make hotel reservation and book air tickets;- Other duties may be assigned.Requirements:- Bachelor or above Degree;- Good professional, organizational and interpersonal skills;- Good oral and written communication skills;- Good English both in written and verbal (Band 4 is a MUST);- Ability to work independently, self-starter, work under pressure, accept responsibilities and learn new tasks;- Proficiency with Microsoft Word, Excel, Power Point and other software packages;- Prior pharmaceutical or medical experience is desirable;- Have some basic knowledge about clinical research. 职能类别： 其他 行政专员/助理 关键字： Project Assistant, Research Assistant, Clinical Trial Assistant, CTA
联系方式
上海市徐汇区漕溪北路398号汇智大厦502室
公司信息
Chelsea Clinical Research is a Shanghai-based Contract Research Organization (CRO) which provides a comprehensive range of clinical trial services to international pharmaceutical companies, biotechnology companies and research institutions in China. Our mission is to deliver service excellence and timely, quality results for our clients. As a professional drug development organization, we believe in the value of building trusted parternership with our clients.
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