| |
|
| 单位名称： |
精鼎医药研究开发（上海）有限公司
|
| |
|
| 需求专业及人数： |
统计编程师 Statistical Programmer
工作职责：
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.
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 high quality derived datasets, tables, figures and data listings.
职位要求：
Educated to BS or above degree level in the relevant discipline is preferred or equivalent work experience. (Statistics, Pharmacy, Mathematics, Mathematics, Computer Science, Biological science, 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
医学编辑Associate Medical Writer
工作职责:
Upon completion of training, the Associate Medical Writer will provide technical and administrative support during preparation of all clinical documents (ICF, CSR, Narratives, Safety report, etc).
Assistance in production and distribution of Medical Writing project materials, word processing documents or edits to documents, formatting, tabulation, and pagination of documents, compilation of report appendices, preparation and maintenance of Medical Writing Services electronic project files and archiving of project materials. The Associate Medical Writer must be conscientious, able to work with minimal supervision, have an aptitude for working with a variety of different software packages, exhibit a high degree of flexibility and initiative, demonstrate the ability to follow up on multiple tasks and projects, and possess the ability to handle matters of a confidential nature.
职位要求：
Excellent interpersonal, verbal and written communication skills
Client focused approach to work
A flexible attitude with respect to work assignments and new learning
Ability to manage multiple and varied tasks with enthusiasm and prioritize workload with attention to detail
Willingness to work in a matrix environment and to value the importance of teamwork
Knowledge of word processing, spreadsheet, database and e-mail applications desirable.
|
| |
|
| 招聘要求： |
.
|
| |
|
| 选聘方式： |
其它
其它方式
|
| |
|
| 学历层次： |
专科及以上
|
| |
|
| 单位通讯地址： |
北京市朝阳区朝外大街12号昆泰国际中心11层0-1101、1115号
|
| |
|
| 邮政编码： |
.
|
| |
|
| 单位固定电话： |
.
|
| |
|
| 单位移动电话： |
.
|
| |
|
| 单位传真电话： |
.
|
| |
|
| 单位联系人： |
.
|
| |
|
| 单位网址： |
ww***com[点击查看]
|
| |
|
| 单位电子邮箱： |
iris.chen@ 或 vivian.wang@parexel.co
|
| |
|
| 单位介绍： |
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50多个国家，并设有70多家分支机构，全体员工超过12000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：
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 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。欲了解更多公司信息，请访问：ww***com[点击查看]
|
| |
|
| 单位所在地域： |
北京市朝阳区
|
| |
|
| 面试时间： |
|
| |
|
| 面试地点： |
.
|
| |
|
| 备注： |
福利政策
保险类：
社会保险(依照国家规定)及住房公积金 ；
团体保险（包括寿险、意外暨医疗保险）；
补充商业医疗保险；
补充住房公积金。
制度类：
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；
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；
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：
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；
一年可享12天不扣薪病假；
员工旅游,年度体检。
宣讲安排
四川大学、华西医学中心 2014年10月14日14:30 华西校区东园、逸夫楼学术报告厅
|
| |
|
|
