各位网友，现在我公司有SAS程序员和统计分析师的职位，外企医药公司，主要从事临床试验数据的分析。具体的Job Description如下，如果有兴趣的人，请附上您的简历到邮箱xju_ql@sina.com，我会立刻跟您联系。

The role of the post holder is to assist in the provision of a Statistical Programming service. The primary activity of the Statistical Programmer is to develop and review SAS® programs and output for the management and reporting of clinical trial data.

A.  Duties and Responsibilities:

¨       Ensure quality of personal work.

¨       Interact with project team members in related disciplines e.g. Clinical Data Management, Clinical and Biostatistics.

¨       Prioritize personal workload to meet specified completion dates.

¨       Display a positive attitude at all times, promoting and contributing to a good team spirit with a productive and professional environment.

¨       Develop good problem solving skills and a willingness to learn and seek advice from senior Statistical Programming staff.

¨       Acquire knowledge of other aspects of the work of a Statistical Programmer Analyst under the supervision of the senior Statistical Programming staff.

¨       Perform other duties as assigned by senior Statistical Programming staff.

¨       Carry out all activities according to SOPs working within the framework of the Quality Management System and to Good Clinical Practice (GCP).

¨       Develop and review SAS programs and output as required for the management of clinical trial data, the tabulation of data, preparation of patient data listings, graphical output, creation of derived datasets and statistical analysis of data as specified in the Statistical or Report Analysis Plans.

¨       Develop programs for ad hoc tables and listings. Write, modify, and maintain programs that produce diagnostics and listing for data review in support of Data Management.

¨       Carry out electronic data transfer (both incoming and outgoing. Develop programs for data transfers and assist in their review to ensure the data transfer has been produced to specification.

¨       Set-up utilities/SAS based systems to assist and facilitate Clinical Data Management activities.

¨       Review draft and final production runs for projects to ensure quality and consistency.

B.   Language Skills Required:

¨       Speaking:              Yes        English, Chinese

¨       Writing/Reading:   Yes        English, Chinese