Resume

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CURRICULUM VITAE RAHUL GURRAM Mobile: +91 7396355850 Email: [email protected] Career Objective “2+ years of professional experience of SAS programming in Clinical and Pharmaceutical Industries. Professional Snapshot Experienced in handling complex processes using SAS/BASE, SAS/MACROS, SAS/ACCESS, SAS/SQL, SAS/ETL and SAS/GRAPH. Experience in generating Reports employing various SAS data steps and proc steps such as DATA_NULL_, PROC REPORT, PROC TRANSPOSE. Generated Tables, Listings and Graphs as per company standards and in compliance with 21 CFR Part 11, FDA and other regulatory guidelines. Experience in generation of Tables, Listings and Graphs by using SAS/ Base, SAS/Graph and SAS/STAT on different phases of clinical Trials. Interacted with senior Bio-Statisticians in analyzing the data, generating reports like tables, listings and graphs. Exposure to clinical trial data such as demographic data, Adverse Events(AE), Physical Examinations, concomitant medications, Laboratory data (Lab data) and Vital Signs. Worked on phase-II, Phase-III clinical trials, performed clinical data analysis and generated SAS reports in accordance with the SOPs and guidelines. Proficiency in using statistical procedures like proc freq, proc ttest, proc univariate, proc anova, proc NPar1Way. Knowledge of CDISC processes such as SDTM. Good skills, commitment, result oriented, hard working with a quest and zeal to learn New technologies. Skills Summary

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Transcript of Resume

Page 1: Resume

CURRICULUM VITAE

RAHUL GURRAMMobile: +91 7396355850

Email: [email protected]

Career Objective

“2+ years of professional experience of SAS programming in Clinical and Pharmaceutical Industries.”

Professional Snapshot

Experienced in handling complex processes using SAS/BASE, SAS/MACROS, SAS/ACCESS, SAS/SQL, SAS/ETL and SAS/GRAPH.

Experience in generating Reports employing various SAS data steps and proc steps such as DATA_NULL_, PROC REPORT, PROC TRANSPOSE.

Generated Tables, Listings and Graphs as per company standards and in compliance with 21 CFR Part 11, FDA and other regulatory guidelines.

Experience in generation of Tables, Listings and Graphs by using SAS/ Base, SAS/Graph and SAS/STAT on different phases of clinical Trials.

Interacted with senior Bio-Statisticians in analyzing the data, generating reports like tables, listings and graphs.

Exposure to clinical trial data such as demographic data, Adverse Events(AE), Physical Examinations, concomitant medications, Laboratory data (Lab data) and Vital Signs.

Worked on phase-II, Phase-III clinical trials, performed clinical data analysis and generated SAS reports in accordance with the SOPs and guidelines.

Proficiency in using statistical procedures like proc freq, proc ttest, proc univariate, proc anova, proc NPar1Way.

Knowledge of CDISC processes such as SDTM. Good skills, commitment, result oriented, hard working with a quest and zeal to learn

New technologies.

Skills Summary

SAS Tools : SAS/BASE v9.2, SAS/MACROS, SAS/connect, SAS/Access, SAS/STAT, SAS/GRAPH, SAS DI Studio 4.2

Databases : Oracle11g.Operating Systems : MS-WINDOWS.

Professional experience

Working as a Clinical SAS Programmer from Aug 2011 to till date.

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Professional Experience:

Project Details: Project # 3: Project Title : A phase-II, open-label, multicenter study of single drug. Role : Clinical SAS Programmer. Duration : From July 2013 to till date. Therapeutic Area: Oncology Roles and Responsibilities:

Provide SAS programming expertise in producing ADS, Tables, Listings and Graphs from clinical trial data.

Develop, modify and validate SAS programming work according to Statistical Analysis Plan (SAP).

Prepared efficacy and safety summary results with tables, listings, graphs.

Performed Statistical Analysis using SAS/STAT procedures like PROC ANOVA, PROC GLM, PROC REG, PROC CORR, PROC TTEST, and PROC NPAR1WAY.

Worked on datasets like Demog, AE, Vitals, Conmed, Physical Examination, Labs.

Generate reports, listings and graphs using SAS/BASE, SAS/MACRO, SAS/SQL and SAS/STAT.

Create reports in PDF and RTF format using SAS Output delivery system ODS.

Used functions like Compress, Substr, Scan etc to Manipulate Data.

Project #2: Project Title : A Phase-II, Multicenter, Randomized Study for Type- II Diabetes. Role : Clinical SAS Programmer. Duration : From Aug 2012 to June 2013. Therapeutic Area: Diabatology Roles and Responsibilities:

Performed data analysis, statistical analysis, generated reports, listings and graphs using SAS/BASE, SAS/MACRO and SAS/GRAPH, SAS/SQL, SAS/STAT.

Validating the data and developing SAS programs to created study specific datasets which are used as source datasets for generating reports.

Modifying existing datasets using set, sorting, merging techniques.

Produced customized reports by using data _null_ and also provided descriptive statistics using PROC MEANS, PROC FREQ, and PROC UNIVARIATE.

Created SAS output report to RTF, PDF format using Output Delivery System (ODS).

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Project #1: Project Title : A Phase-III, multicenter double blind randomized controlled study. Role : Clinical SAS Programmer. Duration : From Aug 2011 to July 2012. Therapeutic Area: Cardiology.

Roles and Responsibilities:

Created analysis datasets by using Base SAS. Developed programs to generate various Safety and Efficacy reports. Generated tables, listings, graphs for the clinical trial study Worked closely with the research team of scientists to analyze the data, generate the

reports, and list them according to specifications. Making the data ready for analysis using SAS/Stat procedures like Proc means, Proc

freq, Proc univariate, Proc ttest, Proc Anova etc. Created Clinical trial reports using Proc Report Used functions like Compress, Substr, Translate, etc to Manipulate Data.. Used SAS/Base procedures like Proc freq, Proc Transpose, Proc copy, Proc Format.

Professional Qualification

B.Pharmacy from OU during the year of 2006-10 at Hyderabad.

Declaration: I hereby solemnly affirm and declare that the above facts are true to the best of my knowledge and belief.

Place:Date:

(G.RAHUL )