SAS Programmer Resume

OBJECTIVE

An energetic and dependable team player with strong programming skills and abilities is seeking a stimulating and challenging position to work as a SAS programmer in health science area and Comfortable working alone or in a team environment.

PROFESSIONAL SUMMARY

Worked extensively with various SAS modules like SAS/BASE, SAS/MACROS, SAS/ STAT, SAS/ACCESS and SAS/SQL.
Strong experience in various SAS procedures like Sort, Contents, Freq, Means, Format, Univariate, Transpose, Report, Copy, Compare, SQL and data _NULL_ statement.
Good experience in using SAS/GRAPH procedures exclusively PROC GPLOT.
Generated TABLES, LISTINGS and GRAPHS as per company standards.
Good Knowledge in understanding the PROTOCOLS, SAP, SOP and CDISC Process (SDTM, ADAM, ODM Models).
Have fundamental understanding of clinical research and ICH-GCP guidelines.
Generated output files in RTF & HTML format using SAS/ODS.
Experienced in working closely with data managers and statisticians to provide SAS Programming in analyzing Clinical Trials to generate Tables, Listings, Graphs, and Validations.
Strong experience in Phases II of clinical trials including safety reports, and efficacy summary for FDA submission.
Excellent knowledge of SAS programming, associated features and their applications in pharmaceuticals industry environment in particular clinical trial data setting.
Excellent communication and interpersonal skills, have worked with professional colleagues and staff in a team-oriented, deadline driven environment.

EXPERIENCE SUMMARY

2+years of experience as a Clinical SAS Programmer.
Working as a Clinical SAS Programmer in CLINI TRIAL, Hyderabad

SKILLS

SAS Tools : SAS/BASE, SAS/MACROS, SAS/SQL, SAS/STAT,
SAS/ODS, SAS/GRAPH, SAS/ACCESS.
Operating Systems: Windows 2010, Linux/Unix., XP, Vista, Microsoft Office.

EDUCATION DETAILS

Bachelor of Pharmacy

PROJECT DETAILS

Confidential,Designation : SAS Programmer.
Responsibilities:

Understanding of clinical trial data and hands on in data manipulations.
Working closely with Data Management group to assure data quality by providing ad-hoc analysis.
Modifying existing datasets using set, sorting, merging techniques using SAS/Base and SQL.
Making the data ready for analysis using SAS/Stat procedures like Proc means, Proc freq, Proc Univariate, Proc t-test, Proc ANOVA etc.
Creating analysis datasets by deriving the required variables using Base SAS as per the specifications.
Generating tables, listings as per the client specification.
Generate and QC summary tables, data listings and graphs for in-house analyses of study data.
Attended project team meetings, worked with Bio-Statisticians.
Creating rtf and html reports using SAS ODS facility.
Using predefined macros as per the requirement.

Confidential,Designation : Clinical SAS Programmer.
Responsibilities :

Involved in data cleaning, validation activities to assure validity and accuracy of the data.
Generated ad-hoc reports for raw datasets using Print and Report procedures.
Deriving required variables as per the specification to create analysis datasets from raw datasets forclinicaltrials.
DevelopedSASprograms to create study specific datasets, which were used as source datasets for report generation.
Developed reports like tables, listings using proc report.
Created rtf and html files using SAS ODS facility.
Extensively used different SAS procedures such as Proc Means, Proc Univariate, Proc Freq and Proc SQL to make the data ready for analysis.
Writing SAS programs for peer review checks as a Q C programmer.
Comparing the source datasets for report generation using proc compare as part of QC.
Attended project team meetings, worked with Bio-Statisticians.

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