a*******5
发帖数: 8 | 1 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:
• Minimum three years of 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 contact me.
"help others, help yourself" |
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