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文章阅读:SAS Programmer in clinical trials
[同主题阅读] [版面: 天津大学] [作者:analyst15] , 2011年05月09日19:37:32
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发信人: analyst15 (lala), 信区: TJU
标  题: SAS Programmer in clinical trials
发信站: BBS 未名空间站 (Mon May  9 19:37:32 2011, 美东)

Location: South San Francisco

Responsibilities:

•    SAS and Data management programming support with respect to
design, conduct & analysis of clinical trials.
•    mainly responsible for database specification review, data review
and developing data edit checks in SAS.
•    help to prepare analysis datasets, summary tables and graphs for
presentations, manuscripts and reports.

Requirements:

•    Hands-on experience in clinical SAS
programming and data management in biotech/pharmaceutical/CRO
•    Master’s degree in computer science, statistics or related field
.  Good understanding of EDC and CDISC, solid knowledge of BASE SAS, and SAS
MACROs.
•    Detail oriented, excellent validation, documentation and
communication skills.

If you or if you know someone who is interested, please 站内联系。
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