| 查看: 993 | 回复: 12 | |||||||||||
| 当前只显示满足指定条件的回帖，点击这里查看本话题的所有回帖 | |||||||||||
[交流]
Global CRO公司招聘生物统计师Biostatistician - 上海
|
|||||||||||
Accountabilities Develops statistical analysis plans and reporting specifications for simple to moderate clinical studies. • Develops and describes appropriate statistical techniques for the analysis of data in a statistical analysis plan. • Works with other statisticians on statistical methodology, study design, therapeutic area details, and data analysis. • Design appropriate shells and specifications for outputs. Performs statistical analyses and interprets results from simple to moderate clinical studies. • Develops or QCs analysis programs to implement techniques described in the statistical analysis plan. • Approves final database for freeze/lock. • Assesses model assumptions for statistical analyses. • Works with programmers, writers, and clinicians to coordinate data summarization and analysis activities, including summary statistics, tabulations, graphics, analysis output, and raw data listings. • Develops and reviews statistical reports and statistical sections of clinical study reports. Contributes statistical expertise to project teams for the design, analysis, and reporting of simple to moderate clinical studies. • Serves as primary functional representative on project teams. • Provides input into the preparation and review of clinical study protocols. • Creates dummy and final randomization schemes for clinical studies. • Participates in the development and review of CRFs, data edit specifications, and critical variable lists. • Works with the project manager and functional manager to determine resource projections and project schedules. • Visits clients to discuss statistical issues. Maintains, develops, and shares knowledge of company and industry procedures and methodologies. • Performs billable work in accordance with WuXiPRA’s policies, procedures, and SOPs. • Maintains solid knowledge of drug development process. • Maintains solid knowledge of SAS procedures and good programming practices. • Continues statistical training on new methods and techniques via self-study, internal training and courses, and external conferences and courses. • Trains and mentors new or junior statisticians on statistical methods and WuXiPRA procedures. • Develops knowledge of FDA and EMEA guidelines and requirements for reporting of clinical trials data. Qualifications MS degree with 3 years of experience within the clinical trials or pharmaceutical industry or PhD degree in statistics or biostatistics Demonstrated expertise in multiple and complex statistical areas Demonstrated ability to plan, implement, and monitor the statistical processes for clinical studies Excellent written and oral communication skills; Read, write and speak English. If interested in this position, please send your English CV to jerryyoung6@163.com |
回复此楼» 猜你喜欢
274求调剂
已经有20人回复
-
265求调剂
已经有16人回复
-
材料与化工304求B区调剂
已经有6人回复
-
321求调剂
已经有5人回复
-
085600材料与化工306
已经有7人回复
-
085602化学工程求调剂。
已经有4人回复
-
312求调剂
已经有10人回复
-
材料考研求调剂
已经有6人回复
-
调剂推荐
已经有5人回复
-
中国科学院深圳先进技术研究院-光纤传感课题组招生-中国科学院大学、深圳理工大学联培
已经有4人回复
13楼2015-07-07 11:11:24
4楼2015-06-17 14:14:39
6楼2015-06-18 16:09:16
  |
7楼2015-06-19 18:24:18
