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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.
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
Pfizer, Kalamazoo, MI SAS Programmer/Analyst Responsibilities: Jan’07-Till Date
Data Managers. SAS/Graph. PL/SQL. CA SAS Consultant/ Analyst Responsibilities: Jul’04-Aug’05 . UNIX and WIN NT Chemical Diversity Labs Inc. • Used SAS for pre-processing data. data validation. Santa Clara. Graphs and Listings for inclusion in Clinical study reports and regulatory submission. SAS/Graph. REPORT. and Clinical Research Managers as appropriate. graphics and statistical analyses. • Extensively used basic statistical procedures like UNIVARIATE. Oracle 9i. WIN NT Abbott Laboratories .Provided programming support for the creation and maintenance of programs used in data management. SQL queries. SAS/SQL . • Attended project team meetings. and data analysis. • Accessed various database to gather data. SAS/Macros. • Involved in creating Transport-files for electronic submissions to FDA. SUMMARY. Analysis and Report generation. SAS/Access. Univariate. SUMMARY and also provided descriptive statistics using PROC Means. ORACLE. PROC TABULATE and DATA_NULL_. • Involved in clinical trails programming of data tables and listings for reporting on safety and efficiency. • Produced customized reports by using PROC TABULATE. UNIX. • Developed efficient. • Implemented statistical analysis plans and specification documents. Frequency. indexing. SAS/SQL. The generated reports are reviewed and sent to the FDA (Food and Drug Administration). performed a table lookup and translated data values for meaning and readability. TABULATE. Validation. Reviewed and provided feedback for Data Integrity Plans. worked with Bio-Statisticians. and statistical report generation. Environment: SAS/Base. • Downloaded data from Oracle using SQL within SAS to be analyzed and exported to Excel for further analysis. • Used Dynamic Data Exchange (DDE) feature of SAS for importing and exporting of data from and into SAS. MS Access and Excel. RTF using ODS statements and PROC Export. • Created reports in PDF. well-documented. HTML. SAS/Stat. merging on the clinical data and generated reports. MEANS. • Extracting data from different data sources and creating SAS data sets. Tested and debugged existing macros. generating reports. GPLOTS. • Generated Tables. Environment: SAS/Base. readily comprehensible and modifiable SAS code using SAS/BASE and SAS/MACRO facility. CA SAS Programmer Sept’05-Dec’06 • Responsibilities: • Prepared clinical data listings and summaries for statistical analysis and analyzed clinical data using SAS system. PS. SQL. San Diego. ANOVA. • Used Base/SAS to perform sorting. • Developed SAS macros for validating the data from CRF. • Developed reports using PROC REPORTS. • Created complex and reusable Macros and extensively used existing macros and developed SAS Programs for Data Cleaning.
transportable files. Oracle.Reddy’s Laboratories.Manipulated SAS datasets extensively with SAS/BASE and SAS/MACRO. SAS/Graph. SAS/Macros. SQL. • Using extensively ODS. • Involved in writing code using Base SAS & SAS/Macros to extract. • Extensively used Data _Null_ and SAS procedures such as Print. • Tabulation counts. • Created tabular reports using Base SAS & SAS/Report procedures. REPORT. Windows NT Dr. • Generated analysis reports. and SAS/Reports. involved in the update & maintenance of the data warehouse. Freq. • Involved in the pharmaceutical data analysis and created reports by extensive use of Base SAS. medical writers and data managements. SAS/Macros. merging on the clinical data and generated reports. Environment: SAS/Base. • Documenting and archiving programs logs and output. Jul’03. TABULATE. listings and graphics submitted to FDA. Environment: SAS/Base . SAS/Access. PROC REPORT and PROC TABULATE for reporting. SAS/Stat. Developing and modifying SAS programs to produce summary tables. Windows 2000. indexing. Summary and Transpose for producing ad-hoc and customized reports and external files. Oracle. • Generating graphs with PROC GPLOT and PROC GCHART. • Created SAS views from Oracle database tables using SAS/Access and writing SAS programs using Base SAS and SAS/Macros to create SAS reports. UNIX. MS Excel. SAS/Macro. • Wrote SAS edit checks for data verification. Richmond.Jun’04 • . clean and validate data from oracle tables. • Converting data from MS-EXCEL to SAS datasets with PROC IMPORT. • Involved in producing the detail and summary reports using PRINT. Tabulate. Proc Means and Proc Freq. design and development of sales analysis for pharmaceuticals manufacturing and distribution company. VA Data Analyst Responsibilities: • Created data sets using the data from external sources like flat files and Excel spread sheets.Jun’03 SAS Programmer Responsibilities: • As a SAS programmer and analyst. graphs using SAS/Reports. Report. SAS/Connect. Means. correlations and check for dispersion from normality are performed using Proc Univariate. ISS (integrated summary of safety) and ISE (integrated summary of efficacy) for NDA submission. • Involved in system analysis. MEANS and SUMMARY procedures. India Aug’02. • Capital One. • Interacting with statisticians. SAS/SQL. PROC PRINT. • Generating data definition tables. clinicians. SAS/Reports. • Used Base/SAS to perform sorting. • Analyzed data using SAS/STAT procedures.
Environment: Cobol. PDF formats using SAS/ODS. SAS/ODS. code and reports for handing over the project. • Created SAS/Views from Oracle database tables. etc. SAS/Access. . DB2. • • Satyam computer’s. Sept’01. Windows NT.) to get the desired output. SAS/Stat. SAS/Connect. Proactively resolving issues.Documentation of design. merging. Designed flowcharts indicating the input data sets and the techniques that would be used (sorting. SAS/Graph. India Team Member Job Responsibilities: • 24X7 production support.Jul’02 • • • Resolve production issues. Environment: SAS/Base. Oracle 8i. MS Excel. VSAM. UNIX. Providing technical help when required and providing the training where necessary. • Created reports in HTML. JCL. SAS/Macro. RTF .
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