Data Computer Science
Resume:
Dheeraj Errabelly
Email:*********.*******@*****.***
SUMMARY
4+ years as SAS Analyst/Programmer with extensive experience in Data Analysis and
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Reporting in Pharmaceutical Industry.
Extensive knowledge of different phases of Clinical Trials.
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Experience with Base SAS, SAS/Macros, SAS/ACCESS, SAS/GRAPH and SAS/STAT
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and SAS/SQL.
Knowledge of 21 CFR Part 11, and CDISC SDTM, ADaM standards for regulatory
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submissions.
Worked with Statisticians to provide SAS programming in analyzing the Clinical Trial
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Data and generate Tables, Listings and Graphs.
Extensively worked on different PROCs, PROC TRANSPOSE,PROC UNIVARIATE,
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PROC FREQ, PROC MEANS, PROC SUMMARY, PROC COMPARE, PROC REPORT,
PROC DATASETS, PROC FORMAT and PROC SQL etc.
Assist in Creating Regulatory submission documents like SAS Transport Files,Data
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definitions document, CRF annotations.
TECHNICAL SKILLS
SAS Tools: SAS/BASE, SAS/MACROS, SAS/STAT, SAS/GRAPH, SAS/SQL,
SAS/ODS
Languages: SAS, SQL, PL/SQL, HTML, C
Database: MS Access, MS SQL Server 2000
Operating Windows XP, MS DOS 6.22, UNIX
System:
Office tools and MS Office, Lotus Notes, Adobe Photoshop, IDBS Activity Base and SARgen
other Software (Database management MS ACCESS).
Packages:
PROFESSIONAL EXPERIENCE
Clinical SAS Programmer (February2009 – Present)
Progenics Pharmaceuticals, Inc., NY.
Responsibilities:
Provided SAS programming and analysis support for Phase II-III clinical trials.
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Generated safety tables (Adverse Events, Patient profile, Demographic listing, Vital
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Signs, Reason for withdrawal by treatment).
Generated high quality reports in the form of listing and RTF using SAS ODS.
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Primary programmer to produce tables, listings, and figures for the clinical study report
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(CSR).
Secondary programmer to validate SAS programs that produce derived-analysis datasets
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and data analyses.
Worked closely with Study statisticians to implement the analysis specified in Statistical
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Analysis Plan (SAP).
Used SAS/Base, SAS/Stat, SAS/Graph, SAS/Macro to implement statistical analysis
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procedures, generate reports and graphs.
Worked on pre-existing macros for data validation by checking data distribution and
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comparison to standard data.
SAS Programmer (January 2008 – January 2009)
Aderis Pharmaceuticals, Richmond VA
Responsibilities:
Provided SAS programming and analysis support for Phase II-III clinical trials.
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Used SAS/ACCESS to read datasets from Oracle database and also read and write other
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PC File formats.
Provided programming to produce tabulations, graphics, and listings from clinical trial
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data.
Worked on pre-existing macros for data validation by checking data distribution and
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comparison to standard data.
Performed Data manipulation using techniques like merging, appending, concatenating
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and sorting.
Read in different PC File formats to SAS datasets and incorporated them into the clinical
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database.
Generated highly customized reports using SAS macro facility, PROC SQL & Data _null_
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techniques.
Validated, documented and tested component programs in an efficient manner for
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inclusion in integrated reports.
Data Analyst/SAS Programmer (March 2005 – December 2007)
Dr. Reddy’s Laboratories, India.
Responsibilities:
Created SAS programs for generating TLG’s using SAS/BASE, SAS/GRAPH and
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SAS/STAT.
Validated TLG’s using SAS/BASE, SAS/GRAPH and SAS/STAT.
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Developed customized reports using PROC REPORT, PROC FREQ, PROC MEANS and
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DATA _NULL_.
Created Annotated Case Report Forms(CRFs)
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Worked in all three phases of drug development process.
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EDUCATION
B.E, Computer Science & Engineering
JNTU, India.
M.S, Computer Science
Stratford University, Virginia.
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