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[招聘] Excel-PPD招聘生物统计师实习生,上海,硕士,2名

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1#
excelhr 发表于 2009-12-1 10:08:10 | 只看该作者 |倒序浏览 |阅读模式

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实习期3个月以上;实习期间公司将授予相应技能培训,语言培训以及提供英语工作环境;实习期满通过考核可以有机会转为正式员工,享受有竞争力的薪资待遇。
' Q* c2 g3 S/ m" ~; s# F' E任职要求:生物统计相关专业,硕士2010年毕业生,英语熟练
5 p/ ]5 b; K) @- \+ n4 z联系方式:yujie.ma@excel-cro.com
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$ o! Z! ]7 W, ^Performs biostatistical and programming activities for given clinical trials involving drugs, biologics and medical devices; assists higher level biostatisticians for project tasks.
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* E) V2 u8 K4 q' Z; x  m7 }' |% v# S* w0 ^Responsibilities" \4 H2 M5 E& l; N. X( c: O
        Assists in study design and development of statistical section in clinical trial protocols0 I+ @- h: B8 E
        Assists sample size and statistical power calculations and randomization schedule generation: O5 e- D* ~! f& i& m8 A. J* i
        Attributes to development of statistical analysis plans including table shells design for individual studies- u. r8 W5 @  ?! k# u  ^0 y
        Supports data safety monitoring board (DSMB) or data monitoring committee (DMC) and clinical endpoints committee (CEC) regarding to statistics analysis
* @0 O1 z; ?9 I' I  A/ X6 X% N        Participate in statistical support for CRF design, database development, data validation plan and blinded data review . X5 j4 l5 f, _, S$ ^$ _+ _4 ?& H
        Performs SAS programming to generate tables, listings, figures, and statistical analyses, i+ u  U: o3 u; l$ j
        Assists higher level biostatisticians for the project tasks
7 `% {3 y8 @) c# Z        Conducts literature searches to support statistical team/ H  c) H0 K$ H' G0 y6 w
        Performs other duties assigned by supervisor
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" W, U# K0 u  s& W6 V4 E) OQualifications  _/ |$ y- Z: ], D
        An advanced degree (Ph.D. or M.S.) in biostatistics, statistics or related field$ B* ]9 Z9 V$ e* F% m- M5 ]
        Experience of statistical analysis in the pharmaceutical industry is preferred( h* }0 A/ V1 b! i+ H/ |
        Ability to deal with sensitive inquiries or complaints from clients or potential clients and to protect confidentiality
0 `$ M) O! h' C& F3 J$ U* a        Be knowledgeable in drug agencies (e.g. FDA) regulations and requirements governing the conduct of drug and medical device studies including, but not limited to, GCP and ICH requirements
0 H$ a8 o7 K9 T" O8 c9 y' f' a        Good communication and interpersonal skills  w! H8 H8 [& k! C. o
        Proficient working in a PC/Windows environment
5 @# L1 K! @3 c* |        A good command of English language if one’s native language is not English
2#
sparklem65 发表于 2009-12-1 16:46:41 | 只看该作者
感谢分享,很不错的
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3#
蜜豆牛奶冰 发表于 2009-12-2 22:12:41 | 只看该作者
帮顶一下~~~~~~~~
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