Resume of Clinical SAS programmer Available for Projects

Here is details of Clinical SAS programmer available with me immediately. He is in NJ.
He can go for Contract jobs. He can relocate anywhere in US & go for face to face.
Mail me the job on shalin.sutaria@cyberthink.com Please add me to your req. distribution too.


PROFESSIONAL SUMMARY:
*       Certified SAS programmer
*       Over FIVE years of experience working with the statistical departments of pharmaceutical, and contract research organizations (CRO).
*       Excellent knowledge of data step programming using SAS/BASE
*       Strong understanding of running Structured Query Language(SQL) using SAS Software's SQL Procedure
*       Proficient in creating of macro variables and macro programs using SAS Macro Language
*       Strong knowledge of importing data from various sources such as ASCII files, EXCEL files, Microsoft ACCESS, Oracle, Teradata using various techniques such as data step INFILE statements with MISSOVER/TRUNCOVER       option, PROC IMPORT, SQL Pass-through facility, and LIBNAME statements using SAS/ACCESS interface to Oracle, Teradata, etc.
*       Strong knowledge of bio-statistical procedures using various PROC routines in SAS/STAT such as Pearson's chi-squared test, Cochran-Mantel-Haenszel tests for independence using PROC FREQ, descriptive statistics using         PROC MEANS, PROC SUMMARY, PROC UNIVARIATE, analysis of variance and complex generalized linear models (GLM) using PROC ANOVA and PROC GLM, PROC CORR, PROC REG, PROC TTEST, Kaplan-Meier survival       curves using PROC LIFE TEST
*       Strong understanding of epidemiological principles including various study designs such as retrospective case control and cohort studies.
*       Exposure on report writing, and creation of Tables, Listings, and Figures using various techniques such as ODS OUTPUT, ODS TRACE , PROC FORMAT, PROC TABULATE, PROC REPORT, DATA _NULL_, PUT statements using   the power of SAS language elements in the data step
*       Strong knowledge of Output Delivery System (ODS) to create reports in PDF, RTF, HTML formats
*       Knowledge of the drug development process with strong experience of analyzing and reporting, Phase I, II, and III of clinical trial data.
*       Knowledge of new drug application (NDA) submission requirements, FDA regulations including 21 CRF part 11 for electronic submission of data, ICH-GCP guidelines, and Clinical Data Interchange Standards (CDISC).
*       Knowledge of CDISC SDTM and CDISC-SDTM IG v 1.1/3.1.1, 1.2/3.1.2
*       Knowledge of Analysis Data Model CDISC-ADaM v1.2
*       Knowledge of coding dictionaries such as  National Drug Code (NDC), Multum, MedDRA, ICD-9-CM
*       Knowledge of Define.pdf and Define.xml to represent different domains in SDTM 3.1.1/3.1.2
*       Experience in creation of ISS and ISE reports for clinical studies
*       Exposure on various steps of project life cycle such as Data Management Plan (DMP), Statistical Analysis Plan(SAP), data extraction, transformation, loading (ETL), summary of findings, and reporting, and presentation.

TECHNICAL SKILLS:
SAS TOOLS:      SAS v 9.x, SAS v 8.1, SAS v. 6.x, SAS/Base, SAS/Stat, SAS/Graph, SAS/SQL, SAS/ACCESS SAS/ODS, SAS/Macros, SAS/Connect, SAS/ETL, SAS/ACCESS.
Operating System:       MS Windows /98/2000/XP/7/VISTA/NT, UNIX.
Programming/Scripting
Languages:      C, Structured Query Language (SQL), HTML, XML, LATeX, BiBTeX.
MS Office:      Word, Excel with analysis tool pack Add In, PowerPoint, Access and Outlook.
Database:       Oracle Clinical, MS Access

Thanks,
Shalin Sutaria
cyberThink Inc
1125 US Hwy 22 STE 1
Bridgewater, NJ - 08807-2939
Tel: 877-223-7153 ext 634
Fax: (908) 429-8005
mailto:shalin.sutaria@cyberThink.com

cyberThink has been recognized as one of the fastest growing IT Services and Staffing companies in the U.S. by INC. magazine, Deloitte & Touche and Purple Squirrel. cyberThink is an Equal Opportunity employer.