Kiran (732)-857-0547 kaykay005@gmail.

com Summary

Over 6 years of professional experience with 5 years extensively in SAS programming on Unix and windows platforms. Has good experience in full life cycle of project development including designing, development, testing, debugging, documentation, reporting and deploying the applications. Good experience in SAS programming using SAS/Base, SAS/Connect, SAS/Access, SAS/Graph, SAS/Macro, SAS/SQL, SAS/ Stat. Has a good command in generating reports employing various SAS procedures like Proc Print, Proc report, Proc SQL, Proc Summary, Proc Freq, Proc tabulate, Proc Means, Proc Univariate, and Proc Format etc. Created Macros to improve the efficiency of report generation programs. Extensive experience with concatenating, interleaving, and merging SAS datasets. Modified existing SAS programs and created new programs using SAS macro variables to improve ease and speed of modification as well as consistency of results. Worked on clinical trials and has good knowledge in Clinical phase I to IV, including FDA guidelines and formats including 21 CFR part 11. Experience in SAS with Oracle / Access connectivity. Excellent communication skills used to inform, educate, motivate, and interact with industry leaders, co-workers, and clients.

Technical Skills
SAS Skills SAS Procs Other Languages DBMS Operating Systems : SAS 8.2, SAS 7.1, SAS 6.12 (BASE, STAT, ASSIST, ACCESS, MACROS, CONNECT, GRAPH, SHARE). : SQL, Report, Print, Means, Univariate, Corr, Reg, Tabulate, Freq, Convert, Chart, Sort, Summary, Contents, Format, Import, Export, Append, Transpose, Plot, Calendar, Explode, Compare, ANOVA etc. : C, C++, Java : Oracle 9i, MS-SQL Server, MS Access. : UNIX, Z/OS, Windows NT, 98/2000, XP

Professional Experience
Pfizer, Kalamazoo, MI SAS Programmer/Analyst Responsibilities: Jan07-Till Date

Provided programming support for the creation and maintenance of programs used in data management, data validation, and statistical report generation. Extracting data from different data sources and creating SAS data sets. Developed SAS macros for validating the data from CRF. Extensively used basic statistical procedures like UNIVARIATE, SUMMARY, TABULATE, MEANS, GPLOTS. Created reports in PDF, HTML, PS, RTF using ODS statements and PROC Export. The generated reports are reviewed and sent to the FDA (Food and Drug Administration). Used Dynamic Data Exchange (DDE) feature of SAS for importing and exporting of data from and into SAS, MS Access and Excel. Created complex and reusable Macros and extensively used existing macros and developed SAS Programs for Data Cleaning, Validation, Analysis and Report generation. Tested and debugged existing macros. Generated Tables, Graphs and Listings for inclusion in Clinical study reports and regulatory submission. Used Base/SAS to perform sorting, indexing, merging on the clinical data and generated reports. Involved in creating Transport-files for electronic submissions to FDA. Attended project team meetings, worked with Bio-Statisticians, Data Managers, and Clinical Research Managers as appropriate. Reviewed and provided feedback for Data Integrity Plans. Environment: SAS/Base, SAS/Stat, SAS/Graph, SAS/SQL, SAS/Access, ORACLE, SQL, UNIX, WIN NT Abbott Laboratories , Santa Clara, CA SAS Programmer Sept05-Dec06

Responsibilities: Prepared clinical data listings and summaries for statistical analysis and analyzed clinical data using SAS system. Developed reports using PROC REPORTS, PROC TABULATE and DATA_NULL_. Developed efficient, well-documented, readily comprehensible and modifiable SAS code using SAS/BASE and SAS/MACRO facility. Used SAS for pre-processing data, SQL queries, and data analysis, generating reports, graphics and statistical analyses. Accessed various database to gather data, performed a table lookup and translated data values for meaning and readability. Downloaded data from Oracle using SQL within SAS to be analyzed and exported to Excel for further analysis. Implemented statistical analysis plans and specification documents. Involved in clinical trails programming of data tables and listings for reporting on safety and efficiency. Produced customized reports by using PROC TABULATE, REPORT, SUMMARY and also provided descriptive statistics using PROC Means, Frequency, Univariate. Environment: SAS/Base, SAS/Macros, SAS/SQL , SAS/Graph, ANOVA, Oracle 9i, PL/SQL, UNIX and WIN NT

Chemical Diversity Labs Inc, San Diego, CA SAS Consultant/ Analyst Responsibilities:

Jul04-Aug05

Manipulated SAS datasets extensively with SAS/BASE and SAS/MACRO. Developing and modifying SAS programs to produce summary tables, listings and graphics submitted to FDA. Wrote SAS edit checks for data verification. Interacting with statisticians, clinicians, medical writers and data managements. Converting data from MS-EXCEL to SAS datasets with PROC IMPORT. Generating graphs with PROC GPLOT and PROC GCHART. Using extensively ODS, PROC PRINT, PROC REPORT and PROC TABULATE for reporting. Generating data definition tables, transportable files, ISS (integrated summary of safety) and ISE (integrated summary of efficacy) for NDA submission. Documenting and archiving programs logs and output. Environment: SAS/Base, SAS/Macros, SAS/Access, SAS/SQL, SAS/Graph, Oracle, MS Excel, UNIX, Windows 2000. Capital One, Richmond, VA Data Analyst Responsibilities: Created data sets using the data from external sources like flat files and Excel spread sheets. Extensively used Data _Null_ and SAS procedures such as Print, Report, Tabulate, Freq, Means, Summary and Transpose for producing ad-hoc and customized reports and external files. Involved in producing the detail and summary reports using PRINT, REPORT, TABULATE, SQL, MEANS and SUMMARY procedures. Tabulation counts, correlations and check for dispersion from normality are performed using Proc Univariate, Proc Means and Proc Freq. Used Base/SAS to perform sorting, indexing, merging on the clinical data and generated reports. Environment: SAS/Base , SAS/Stat, SAS/Reports, SAS/Macros, SAS/Connect, Oracle, Windows NT Dr.Reddys Laboratories, India Aug02- Jun03 SAS Programmer Responsibilities: As a SAS programmer and analyst, involved in the update & maintenance of the data warehouse. Involved in the pharmaceutical data analysis and created reports by extensive use of Base SAS, SAS/Macro, and SAS/Reports. Involved in system analysis, design and development of sales analysis for pharmaceuticals manufacturing and distribution company. Involved in writing code using Base SAS & SAS/Macros to extract, clean and validate data from oracle tables. Created tabular reports using Base SAS & SAS/Report procedures. Created SAS views from Oracle database tables using SAS/Access and writing SAS programs using Base SAS and SAS/Macros to create SAS reports. Generated analysis reports, graphs using SAS/Reports. Analyzed data using SAS/STAT procedures. Jul03- Jun04

Documentation of design, code and reports for handing over the project. Designed flowcharts indicating the input data sets and the techniques that would be used (sorting, merging, etc.) to get the desired output. Created reports in HTML, RTF , PDF formats using SAS/ODS. Created SAS/Views from Oracle database tables. Environment: SAS/Base, SAS/Macro, SAS/Stat, SAS/Graph, SAS/Connect, SAS/Access, SAS/ODS, MS Excel, Oracle 8i, UNIX, Windows NT.

Satyam computers, India Team Member Job Responsibilities: 24X7 production support.

Sept01- Jul02

Resolve production issues. Proactively resolving issues. Providing technical help when required and providing the training where necessary.

Environment: Cobol, DB2, VSAM, JCL.