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Data Engineer

Location:
United States
Posted:
August 24, 2012

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Resume:

. Competent and committed Programmer Analyst with 3 Years 9 months of

experience working for a major US client at Endosoft, Bangalore

. Good experience in Data extraction, Preparation, Validation and

analysis of various management applications using SAS & Excel

Software.

. Experience in SAS/BASE, SAS/SQL, SAS/ODS, SAS/ACCESS, AND SAS/MACRO.

. Having good experience on ORACLE CLINICAL

. Responsible for accessing and managing data and for performing complex

queries and analysis.

. Extensive programming experience with various procedures like PROC

FREQ, PROC SUMMARY, PROC TABULATE, PROC REPORT, PROC FORMAT and PROC

SQL.

. A consistent track record of successfully employing best business

practices that improve efficiency, reduce operating costs whilst

increasing productivity, all to tight time scales and within budget.

. Experienced in creating reports in PDF, HTML, RTF formats using ODS

statements

. Fine analytical, inter-personal & communication skills with experience

in interacting with clients, multiple user groups and managing

development teams. Ability to work in a fast paced environment and

under deadlines.

. Working as a Clinical Documentation Analyst at Endosoft Solutions Pvt

Ltd, Bangalore from Jan' 2011 to till date.

. Worked as a Content Engineer for Griha Software, Bangalore from Oct'

2008 to Jan' 2011

SAS Products : SAS/BASE, SAS/MACROS, SAS/SQL,

SAS/STAT, SAS/ODS

[Data Extraction; Data Validation;

Data Modification; Data Management;

Data Analysis & Data Reporting using

DATA & PROC Steps in SAS]

Languages : SAS, C, SQL, HTML

Tools : MS Office - EXCEL; POWERPOINT;

WORD; OUTLOOK

Databases : MS-Access, ORACLE CLINICAL

Operating Systems : Windows 95/98/ XP, MS-DOS

SAS BI Tools : SAS/Enterprise Guide

Project - 1:

Domain: Clinical Data Management

Title: Analysis of Phase III Data

Environment: SAS/Access, SAS Base, SAS/SQL, SAS/Graph, SAS/Stat

Project Description

Data of Clinical trial (Phase III) involved a Randomized, Double-Blind,

Placebo Control, Safety/Efficacy Study, The CRF's were provided by Client.

The data is entered into Excel sheets and flat files. Creation of datasets

and cleaning, manipulation, validation of data is done using data step and

BASE SAS procedures. Reports were generated in list files. Reports were

generated on Demographics, Safety analysis, Efficacy analysis and Baseline

characteristics in the SAS system.

Roles &Responsibilities

? Prepared new Datasets from raw data files using Import Techniques and

Modifying existing datasets using SET, MERGE, SORT, and FORMATS.

? Cleaning of data using Data Step and SAS/BASE Procedures.

? Assigned formats and labels to the variables in analysis data sets.

? Generated tables, listings and graphs according to Protocol.

? Creating summary tables using PROC REPORT and PROC TABULATE.

< M.Sc. Biotechnology in 2007 from Bangalore University.

< B.Sc. Biotechnology in 2005 from Bangalore University.

< Higher Secondary Standard in 2000 from Rajasthan Education Board.

< Secondary Standard in 1998 from Rajasthan Education Board.

< P.G Diploma in Clinical Data Management.

Gender : Male

Marital Status : Married

Nationality : Indian

Current Location : Bangalore

Languages Known : English, Hindi

CHANDRESH CHOUBISA

Summary - Total Experience 3 years 9 months

Work Experience:

Technical Skills:

Project Experience

Education & Certification

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