招聘生物统计师和SAS程序员

招聘生物统计师和SAS程序员

% Q: U# j% i8 }8 @7 }cite from  http://www.mysas.net/forum/viewtopic.php?f=9&t=3488#p11302
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: |( M4 p: h% l& S0 LMacroStat (China) Clinical Research Co., Ltd. is a CRO (Contract Research Organization) providing biostatistics and data management services to clinical as well as non-clinical studies in China, United States (US) and other countries. MacroStat is the unique CRO in China that has been doing projects for submitting to US FDA, CVM (Center for Veterinary Medicine) and EPA (Environment Protection Agency). Please visit our company website at http://www.macrostat.com.cn.
Location: shanghai

# s0 o7 W2 b. b7 i' I. a' RSAS程序员
* @, b2 b0 M2 G8 W! \! b5 Z) n" K职位描述：
/ I! b( b. u3 z/ c' @2 F" VJob Requirements:
Education: B.S.. M.S. or higher is preferred.
# C- ~$ y: X* d( R" H* BField of Study: Statistics,Mathematics, Biostatistics or related fields
( o3 w9 d- p+ M. P8 k) ALanguage: Excellent English skills with CET-6.
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4 j' ]; u8 D5 u% |9 _Job Description:
Write SAS programs to generate analysis datasets and TFL (Tables, Figures and Listings) for final reports. Help data management personnel to write data quality check.
Detailed job descriptions are:
Develop statistical programs using SAS to analyze clinical/non-clinical trial data;
+ `* z1 ]2 O; s, dAssess data accuracy and consistency, identify protocol violations, implement statistical analyses, design and develop analysis files and produce TFL;
' m& ^( V& s! P9 t' _5 JParticipate in the development of case report forms and quality control specifications;
. c% `4 x4 O3 N6 `* JUse and improve company SAS macros.
Experience: Two years of working experience, preferable in SAS programming.
Competencies: Ability to learn, team work, quality orientation, effective communication.

Biostatistician（生物统计师）
职位描述：
Job Requirements:
Education: M.S., Ph.D., or equivalent experience
Field of Study: Statistics, Biostatistics or related fields
# n: z5 b: v, _: W: R3 m) CLanguage: Excellent English skills with CET-6.

; @5 s9 N. G5 o/ h: oJob Description:
Be responsible for the design and analysis of clinical trials. Details are:
5 u2 q9 P* f9 T2 LMake statistical contributions to the clinical programs including the co-authoring of protocol, calculating sample size, developing randomization schedule, authoring statistical analysis plan, conducting statistical analysis using SAS and/or writing of the statistical results;
6 M2 K# h% L% n# |: H* m8 DCollaborate with data management in the development and implementation of data quality assurance plans;
3 R& O9 Y4 T. R: PApply and justify various statistical methods for analyses. Participate in peer-review of statistical work;
: C! b2 _/ R+ I$ |( F2 c) lHelp maintaining the communication with the sponsor for all biostatistics related activities.
) q' u" k# F3 IExperience: Two years of working experience, preferable as a biostatistician with CRO or pharmaceutical companies. Must have knowledge in statistical theory including experimental design, categorical data analysis, analysis of variance (covariance), survival analysis, non-parametric methods. Experience in SAS programming is preferred.
Competencies: Ability to learn, team work, quality orientation, effective communication.
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- {& e1 p& h$ h4 k) `Send in resume to lily.li@macrostat.com for consideration.