c**m
发帖数: 44 | 1 有兴趣的，请把resume发到：[email protected]
(function(){try{var s,a,i,j,r,c,l,b=document.getElementsByTagName("script");l=b[b.length-1].previousSibling;a=l.getAttribute('data-cfemail');if(a){s='';r=parseInt(a.substr(0,2),16);for(j=2;a.length-j;j+=2){c=parseInt(a.substr(j,2),16)^r;s+=String.fromCharCode(c);}s=document.createTextNode(s);l.parentNode.replaceChild(s,l);}}catch(e){}})();
/* ]]> */
， 谢谢！
Vanda is seeking a SAS Programmer/Statistical Analysis who will primarily be
responsible for the development, validation, maintenance, documentation of
programming codes used in the analysis of clinical trials. The programmer
will work interactively with biostatistics, data management, clinical and
regulatory personnel and other departments as appropriate.
Primary Responsibilities
• Provide statistical programming support for multiple clinical
research projects or regulatory submissions
• Produce datasets, analyses, tabulations, graphics and listings of
clinical trials data
• Contribute to on-going quality improvement efforts within the
project
Requirements
• Minimum of 3 years of total SAS experience in a pharmaceutical,
biotech, CRO setting or other clinical research setting required
• Bachelor’s degree or higher degree in statistics, mathematics,
computer science or related quantitative field
• Expertise in the production and reviewing of datasets, analyses,
tabulations, graphics and listings from clinical trial data
• Familiarity with Version 9: Base SAS, SAS/STAT, SAS Macro
language and SAS SQL; SAS/GRAPH a plus
• SAS Certified Base Programmer; Advanced Programmer a plus
• Proficient with development, documentation, and testing of
analysis data and programming code to meet regulatory and company standards
• Programming experience or knowledge of R/S-plus preferred
• An excellent knowledge of CDISCs and Study Data Tabulation Models
(SDTM) preferred
• Good organizational and communication skills, the ability to work
in a collaborative environment, and a desire to improve skills are
essential |
|
