[上海]精鼎医药研究开发（上海）有限公司2012招聘

精鼎医药研究开发（上海）有限公司

PAREXEL China Co., Ltd.

 

精鼎医药是一家致力于药物临床试验研究的CRO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的临床研究委托机构（Contract Research Organization: CRO）.(CRO:指一个商业性或学术性的研究机构，试验委托者可将某些工作和职责转移至该机构。)

精鼎医药总公司位于美国，分支机构遍布全球50多个国家，并设有70多家分支机构，全体员工超过10000人，并与亚太地区包括台湾， 韩国，中国（北京，上海，成都，广州），中国香港，印尼，泰国，马来西亚，新加坡，澳大利亚，印度，日本，菲律宾和越南等舍友分公司或办事处，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，并已在业界简历高品质的专业形象以及良好口碑。

服务内容包括：

        新药开发策略的拟定与计划

        国际临床试验规划执行及整合

        临床试验的监测、临床试验数据处理

        临床研究统计分析

        临床试验总结及统计报告

        临床试验稽核服务

        新药查验登记事务

        国际临床试验相关法规咨询等。

精鼎医药（PAREXEL APEX 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。

精鼎医药（PAREXEL APEX 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。

福利制度：

．补贴：
(含车补及饭补)

．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. 补充商业医疗保险                                          4. 补充住房公积金

．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天带薪年假, 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

．员工旅游,年度体检

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。

招聘职位：

临床监察员 CRA

工作职责：

The responsibility of a Clinical Research Associate ( CRA ) is to perform the clinical monitoring aspect of designated projects in accordance with applicable SOPs and regulations.

Performing clinical on-site monitoring activities (drive patient recruitment, source data verification,

drug accountability, data collection), collecting regulatory documentation (when required), performing qualification, initiation, monitoring and termination of investigational sites in accordance with ICH GCP guidelines.

 

职位要求：

 

       Educated to degree level (pharmacy or other health-related discipline preferred).

        Fluent in written and oral English.

        Excellent interpersonal, verbal and written communication skills

        Sound problem solving skills

        Ability to successfully work in team environment

        Able to travel a minimum of 65% on average

 

统计编程师 Statistical Programmer

工作职责：

 

The Statistical Programmer works with close supervision to support various programming activities related to the analysis and reporting of clinical study data.

Deliver best value and high quality service, 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

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 low-medium complexity derived datasets, tables, figures and data listings.

 

职位要求：

       Educated to above degree level in the relevant discipline is preferred or equivalent work experience. (biological science, pharmacy, biological science, mathematics, statistics or other health-related discipline preferred).

        Experience in SAS

        Knowledge of WSOPs/Guidelines/System Life Cycle methodologies, ICH-GCP and any other applicable local and international regulations such as 21 CFR Part 11 and proven practical application

        Knowledge of the programming and reporting process within the Statistical Programming Department

        Good in written and oral English.

        Demonstrate ability to learn new systems and function in an evolving technical environment

        Attention to detail

 

生物统计分析师 Biostatistician

工作职责:

 

The Biostatistician works under the supervision of an experienced biostatistician to assist in the production of statistical reports and the programming of tables, listings and figures.

 

Produce tables, figures and data listings using efficient programming techniques, Perform statistical analyses under close supervision, Assist in the production of statistical reports and statistical sections of integrated clinical reports, Check own work in an ongoing manner to ensure first-time quality, Communicate process improvement ideas within the department, Travel to, attend and actively contribute to all kind of client meetings as appropriate (e.g. presenting and discussing study results accompanying the Biostatistics Lead), Additional responsibilities as defined by supervisor/manager.

 

职位要求：

 

        Above Master in Statistics or related discipline entry level, relevant work experience in statistical analysis

        Good analytical skills

        Attention to detail

        Prior experience with SAS programming desirable

        Competent in written and oral English in addition to local language

        MS in Statistics or related discipline entry level, relevant work experience in statistical analysis

 

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