a*******5
发帖数: 8 | 1 Location: Bay Area
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 PM me.
"help others, help yourself" | h******s
发帖数: 3420 | 2 每次看到这种广告我就奇怪：
有3年clinical programming experience 的人会available 吗？
这些广告上哪去找这样的人啊
review
for
【在 a*******5 的大作中提到】
: Location: Bay Area
: 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
| h*****8
发帖数: 52 | 3 Hi,
Thanks for sharing the information.
I am going to graduate this May from statistics Master program.
I had 2 internship, and currently looking for a SAS programmer position.
May I apply this job?
Thanks,
Shuang
review
for
【在 a*******5 的大作中提到】
: Location: Bay Area
: 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
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