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公司概况


简介


精鼎医药研究开发(上海)有限公司(PAREXEL International)，成立于1982年，是一家致力于药物临床试验研究的CRO (Contract Research Organization)集团公司。总部位于美国，分支机构遍布欧、美、亚、大洋四大洲，且于亚洲13个国家和地区设立了分支机构，致力深耕于当地。精鼎医药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。我们重视与客户的承诺，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。

愿景（Vision）：
创造一个在亚太地区具有国际竞争力的最精良CRO团队。

发展使命（Mission）：
1．争取国际大药厂委托，执行符合国际水准的跨国性临床试验。
2．协助亚太生技及制药产业建立新药开发模式，以提升产品研发能力，幷促使产品国际化。
3．以提升临床试验品质为宗旨，拓展全球市场为目标，整合计算机及通讯科技，在国际上提供客户兼具成本效益及效率的临床试验数据处理中心。
4．建立一个以亚洲人种高发生率疾病的基因数据库，以提供国际性新药研发机构所须之基因信息，协助其缩短药物开发时程，幷提高研发成功率。

公司福利和人才培养计划：
保险类：
1. 社会保险(依照国家规定)及住房公积金；
2. 团体保险（包括寿险、意外暨医疗保险）；
3. 补充医疗保险；

制度类：
1. 学习发展计划 (Learning & Development): 针对个别员工之专业及兴趣，设计符合其个人之生涯规划；
2. 完整的教育训练：每年公司均针对所有员工，提供完整之教育训练；
3. 顺畅的升迁管道及可转调其它部门；如有职缺，亦可申请调至海外各子公司；

请 / 休假制度：
1. 服务第一年即享有14天特休, 后续年休假天数则依据服务年资及公司制度而定；
2. 一年可享12天不扣薪病假；
3. 员工旅游, 年度体检；

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。

应聘方法：
1. 在线投递；
2. 请登录我们的公司网站直投您的简历（http://www.parexel.com/careers/opportunities/）
或投递简历到HR邮箱：claire.gao@parexel.com

我们在收到您的简历之后，会尽快与您联系。

谢谢！

需要怎样的你？

职位信息



Statistical Programmer/SAS Programmer:有SAS经验者优先，招聘各个level的SAS Programmer

Responsibilities:

Deliver best value and high quality service.
Ensure quality control (QC) on all process and technical activities related to:
- trial set-up and maintenance, and/or derived dataset, table, listing, and figure programming and/or implementation of system applications and upgrades/changes to those applications as required in accordance with corporate quality standards, WSOPs / Guidelines, ICH-GCP and/or other international regulatory requirements are performed.
-Check own work in an ongoing way to ensure first-time quality.
-Maintain all supporting documentation for studies in accordance with WSOPs/Guidelines to ensure traceability and regulatory compliance.
-Proactively participate in quality improvement initiatives.
-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.
-Develop wider knowledge of areas of Clinical Data Management Systems (CDMS), Electronic Data Capture (EDC), Clinical Trial -Management System (CTMS), Safety Reporting, SAS and other programming language usage and processes within the GRO, biostatistics, and medical arenas.
-Provide relevant training and mentorship to staff and project teams as appropriate.
-Assist project teams in the resolution of problems encountered in the conduct of their daily work.
-Assist in the coordination of project start-up activities, including Unix/PMED project area set-up, creation of global programs (e.g., setup.sas, formats.sas, etc.), tracking spreadsheets, and required documentation.
-Assist in the production and QC of derived dataset specifications, programming specifications, and other process supporting documents.
-Use efficient programming techniques to produce and/or QC low-medium complexity derived datasets, tables, figures and data listings.

Experience:
First degree (undergraduate or equivalent) in a relevant discipline is preferred or equivalent work experience.
Excellent written and oral communication skills.
Relevant Clinical Trial industry experience is preferred.
Experience working with systems used within the Clinical Trial process (e.g., SAS, CDMS, EDC (Inform, RAVE, DataLabs), CTMS, Medical Safety Reporting)