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精鼎医药研究开发(上海)有限公司招聘简章
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精鼎医药研究开发(上海)有限公司 2017届校园招聘简章
PAREXEL China Co., Ltd.
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公司介绍
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公司性质: 外资
公司规模: 1万人以上
所属行业: 临床研究服务机构
工作地点: 沈阳市 和平区 青年大街286号华润大厦10F? 1007&1001-1002
联系电话:024-3135 2399
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精鼎医药是一家致力于药物临床试验研究的CRO(Contract Research Organization)集团公司,成立于1982年,协助世界各国各大药厂从事新药研发及临床试验。
精鼎医药总公司位于美国,分支机构遍布全球51个国家,并设有80家分支机构,全体员工超过18,660人,并于亚太地区包括中国台湾, 韩国,中国(北京,上海,成都,广州,沈阳),中国香港,印尼,泰国,马来西亚,新加坡,澳大利亚,印度,日本,菲律宾和越南等设有分公司或办事处,提供客户最专业和符合国际标准的临床研究委托服务。目前精鼎医药已成为亚太地区及国内规模最大,服务项目最完整的专业CRO公司,并已在业界建立高品质的专业形象以及良好口碑。
服务内容包括:
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精鼎医药(PAREXEL International)由一群具有丰富跨国性临床试验研发经验及专业知识的精英所组成,服务团队集合各种不同专业领域的人才,包括:药理、毒理、分子生物、生物化学、生物统计、新药研发、临床医师、临床研究、药物法规、药物管理、项目管理及临床试验等等。
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欲了解更多公司信息,请访问:ww***com[点击查看] ?
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福利政策
精鼎医药(PAREXEL International)重视与客户的承诺,更重视人才的培育和养成,我们提供完整的教育训练、职涯规划、优于市场的薪资福利、良好工作环境,期许同仁与公司一同成长,迈向未来。
.保险类:
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.制度类:
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.请 / 休假制度:
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.员工旅游, 员工年度体检
职位信息
精鼎医药因公司业务之需求,开放以下职缺。精鼎医药将以培养国际性的人才为目标,欢迎具有国际观之人才加入。
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统计编程师 Statistical Programmer
Key Accountabilities:
The Statistical Programmer works closely with Data Operation groups to support various programming activities related to the statistical analysis and reporting of clinical study data.
Ensure compliance with WSOPs/Guidelines, ICH-GCP and any other applicable local and international regulations and participate in internal/external audits and regulatory inspections as required, Use efficient programming techniques to produce high quality derived datasets, tables, figures and data listings.
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Education and Skills:
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临床数据分析员Clinical Data Analyst
Key Accountabilities:
The role of the Clinical Data Analyst is to perform assigned tasks or activities in clinical data management. All tasks should be performed in accordance to corporate quality standards or international regulatory requirements.
Activities may include Development of database build specifications, User Acceptance Testing (UAT), data validation and cleaning, generation and integration of queries, running of reports with high levels of direction/supervision, Data reconciliation tasks, Identifying and reporting protocol deviations. Support site monitoring personnel to retrieve missing data as required. Provide work status updates regularly to direct supervisor. Other assigned responsibilities as needed.
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Education and Skills:
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药物安全专员Drug Safety Associate
Key Accountabilities:
Performing clear and accurate data capture of Individual Case Safety Reports (ICSRs) (including serious and non-serious cases from spontaneous and clinical trials origin, literature and E2B cases; and veterinary cases, as applicable) and appropriate medical assessment (including company causality and assessment of expectedness) of ICSRs in accordance with client conventions/guidelines and Standard Operating Procedures.
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Education and Skills:
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简历投递
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邮箱 (邮件主题请注明“姓名 申请职位名称 工作地点”):
Becky.lei@
或
Tony.feng@
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了解更多最新的招聘职位信息,请扫描下方二维码或登录jo***com[点击查看]
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