SUMMARY

• SAS analyst with 8 years of extensive experience in SAS programing.
• Experience in Base SAS, SAS/Macros, SAS/SQL, SAS/Graph, SAS/STAT, SAS/CONNECT, SAS/ODS, SAS/ACCESS.
• Ability to handle projects at every level, to follow Standard Operating Procedures (SOP’s), to perform Data validation Process and to assist in preparing specification.
• Good working experience in Phases I, II and III of the Clinical Trials.
• Good Experience in Cardiovascular, Endocrinology, Oncology, CNS, Infectious disease, Respiratory
• Excellent knowledge of SAS advanced data and file manipulation techniques and SAS Macro’s.
• Ability to follow CDISC data standards like ODM, SDTM, ADaM Standards and maintain SDLC documentation.
• Good Knowledge in 21 CFR - Part 11 Federal law requirements.
• Good Knowledge in Medical Dictionaries like MedDRAand WHO Drug.
• Created, Validate and executed analysis data set Programs.
• Created, Validate and executed Tables, Listings and figure programs.
• Extensive experience in generating ad hoc reports for analysis purpose.
• Extensive Experience in importing and exporting data files to different formats.
• Extensive experience with Concatenating, Interleaving and Merging Datasets.
• Extensive experience in generating reports, listings, tables and summaries for safety and efficacy analysis in specified format using Proc Tabulate, Proc SQL, Proc Report and Proc Template; and validate SAS programs for submissions to FDA (Food and Drug Administration) and other purposes.
• Extensively used different Base SAS Procedures like PROC SQL, PROC IMPORT, PROC EXPORT, PROC CONTENTS, PROC PRINT, PROC SORT, PROC APPEND, PROC REPORT, PROC FORMAT, PROC TRANSPOSE, PROC COMPARE and others.
• Sound knowledge on most of the Procedures in SAS. Extensive familiarity with SAS statistical Procedures including PROC FREQ, PROC MEANS, PROC SUMMARY,PROC UNIVARIATE,PROC TABULATE, PROC TTEST, PROC GLM, PROC ANOVA, PROC REG and others.
• Extensive experience in writing Stored Compiled Macros.
• Thorough Knowledge and experience of Microsoft Office tools like MS Access, MS word, MS PowerPoint, and MS Excel. Extremely energetic, detail oriented, organized team player with strong analytical abilities, communication skills, interpersonal skills, and problem solving skills.
• Highly persistent and motivated with willingness to assume responsibility.

TECHNICAL SKILLS

SAS Tools: SAS 8.0, SAS 9x, SAS/BASE, SAS/GRAPH, SAS/MACROS, SAS/STAT

Statistic software: MiniTab 16

Reporting Tools: SAS/BAS, SAS/GRAPH, SAS/ODS/

Operating Systems: Windows 8.1/7/XP

PROFESSIONAL EXPERIENCE

Confidential, OK

SAS Analyst

Responsibilities:

• As a SAS Programmer generation of clinical data summary tables/Listings/graphs and reports using SAS for Clinical Study Reports for Phases I and II.
• As a SAS Programmer to create SAS datasets from Oracle tables by using SAS/Access, SAS/SQL for analysis.
• Support Data management in data creation/transfers, integrity checks, and audits.
• Develop programming specifications for derived data sets, listing tables and summary tables.
• To clean the data using the SAS Procedures like ProcFreq for Categorical Variables and Proc Univariate for Continuous Variables.
• Clarify the observed issues with Team Leader, Project Manager and Bio- Statistician.
• To perform Quality Checks (QC) for Datasets, Efficacy and Safety Summary Tables, Listings and Graphs by writing Double Programming Method.
• Extensively used Base SAS for data validation and correction.
• Created SAS datasets from raw data for data cleaning and analysis using various Base SAS Procedures.
• Creating permanent formatted SAS data sets and developed reports using Proc Report, Proc Tabulate and DATA NULL for analysis.

Environment: Windows, SQL, SAS/Base, SAS/ STAT, SAS/GRAPH, SAS/ODS, SAS/Macros, SAS/Connect.

Confidential, MD

SAS Analyst

Responsibilities:

• Developed SAS programs to load data from the source and create study specific datasets, which are used as source datasets for report generations.
• Developed macros for report generation using SAS/Macros as per the statistician’s requirements and programs for statistical analysis and data displays.
• Generated Tables, Listings and Graphs for Clinical study Report s for Phases I and II.
• Designed tables, graphs for clinical study reports. Collected requirements from statisticians, prepared requirements document. Used SQL pass-through facility to access the data.
• Created reports in PDF, HTML using ODS statements and Proc Export.
• Extensively used Procedures like ProcFreq, Proc Means, Proc Sort, Proc Print, Proc Tabulate, Proc Report.

Environment: SAS/BASE, SAS/MACRO, SAS/SQL, SAS/GRAPH, SAS/IMPORT SAS/EXPORT, SAS/STAT, SAS/ACCESS, SAS/ODS, Windows.

Confidential, NJ

SAS Analyst

Responsibilities:

• Involved in Phase I and phase II clinicaltrial data analyses.
• Data extraction using SAS/ACCESS and preparing the reports accordingly
• Participated in writing ofclinicaltrial reports (phase II-III), analyzing, and presenting trial results.
• Worked strictly in accordance of Protocol, SAP, Specifications and Client SOPs
• Wrote and reviewed mapping programs, mapping specification and created study datasets from raw data according to CDISC standard SDTM Model
• Developed transport file (.XPT), define file (xml, pdf ) for FDA/NDA submission using SAS XPORT transport format
• Developed batch validation checks (data cleaning) using SAS and automated checks in Oracle clinical CDMS system using SQL
• Analyzed data using SAS/Stat procedures like Means, UNIVARIATE, REG, FREQ, Summary, Report, Tabulate, and SQL
• Generated statistical summary tables, graphs, and patient data listings with statistician
• Participated in preparing Clinical trial reports (phase II-III), analyzing, and presenting trial results and transport files for FDA submission
• Developed safety and efficacy tables for FDA submission
• Developed SAS macros for data cleaning and Reporting and to support routing processing

Environment: Base/SASV9,SAS/STAT,SAS/ACCESS,SAS/Graph,SAS/MACRO, Windows

Confidential

Statistical SAS Programmer

Responsibilities:

• Generated clinical data summary Tables/Listings/Graphs using SAS for Clinical Study Reports for Phase I and Phase II trials.
• Extracted data from RDBMS to SAS by using SAS/Access and SAS/SQL Pass through Facility for analysis.
• Created the derived data to perform analysis as per statistician specifications
• Extensively used SAS/STAT procedures such as Proc ANOVA, Proc GLM and Proc REG to perform statistical analysis on study data
• Cleaned the data using the SAS procedures such as ProcFreq for Categorical Variables and ProcUnivariate for Continuous Variables.
• Used Base SAS procedures such as Proc REPORT, Proc PRINT, Proc CONTENTS, Proc SORT, Proc TABULATE, Proc GPLOT, Proc MEANS
• Clarified the observed issues with Team Leader, Project Manager and Bio- Statistician across the programming.
• Using ods created pdf and rtf output

Environment: Base SAS v8.2, SAS/Macros, SAS/SQL, SAS/Access, SAS/Stat, SAS/ODS, SAS/Graph, Oracle8i, MS Excel, Windows XP.