Sample Clinical SAS Programmer Resume
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JOHN DOE
Street, City, State, Zip code
Tel: (123) 123-1432 | Email: sascrunch@example.com
Dynamic and Result-oriented SAS Programmer with extensive years of SAS programming experience covering all aspects of SAS
processes – analysis, design, testing and validating, including advanced statistical methodologies applied in Pharmaceutical and
Biotech industries (Clinical Environment). Rich background in general linear models, categorical data analysis, survival analysis,
multivariate analysis, design of experiments, longitudinal data analysis, randomized trial designs and survey design and analysis, as
well as creating SAS datasets, macro definitions, debugging programs, and documentation. Possess solid ability in integrating
programing skills, conducting GAP analysis, adapting to new applications and platforms, and converting data from complex clinical
systems.
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SAS Mainframe and SAS Programming
Project Management and Implementation
Database Design and Management
Relationship Management
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SAS Data Warehouse Programming
Clinical Research Analysis
Various Clinical Information Systems
Statistical Documentation and Consolidation
T OOLS AND T ECHNOLOGIES
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SAS Tools:
Statistical Tools:
Database:
Operating Systems:
Web Technologies:
Programs:
SAS/Base | SAS/Stat | SAS/Graph | SAS/SQL | SAS/Access | SAS/ODS | SAS/Report
SAS v 9.x/8.x/6.x | SPSS | R/S-Plus
Oracle Clinical | SQL Server 2000 | PL/SQL | MS Access
UNIX  WINDOWS XP/1998/2000/7
HTML | Adobe Dream Weaver
Microsoft Office Suite (Word, Excel, PowerPoint, Access and Outlook)
P ROFESSIONAL E XPERIENCE
C LINICAL WORLD INC . , New York, NY
Clinical SAS Programmer  Jan 2010-Present
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Oversee the clinical SAS programming and analysis functions and support for the entire clinical studies across
multiple protocols for the submissions such as CSR and Safety
Demonstrate proficiency in coordinating wide range of professional functions such as generating tables, listings, QC
checking, and validating all outputs for Oncology clinical trials; developing reports for Safety and efficacy as per
study requirements; debugging SAS compiling errors and identifying issues; producing reports or analysis data sets;
and SAS data sets and other database management
Play a key role in developing, debugging, and validating the project-specific SAS programs to generate derived SAS
datasets, summary tables, and data listings in accordance with departmental standards
Perform extensive QC (Quality Check) and analysis in reviewing other team members work as well as render
primary support and assistance in data validation and data cleaning in all phases of Clinical studies
Facilitate the modification and development of existing SAS programs as well as accountable for the creation of new
programs using SAS Macros
Work collaboratively with statisticians and clinical data managers in analyzing the Clinical Trials and generating
Reports
Render support in generating analysis data sets and creating specified structure of TLFs through creating Macros
and macro variables using %LET, CALL SYMPUT, and DATA _NULL_
Generate analysis datasets based on the Data Definition Tables (DDT) and in accordance to the CDISC standard.
Used SDTM model (3.1.1)/ ADAM for domain creation and CDISC compliant analysis datasets.
Utilize Proc CDISC for verifying compliance of datasets with CDISC standards and electronic submissions
Experience in working on multiple protocols and/or drug compounds at a time
R E F E R E N C E S AVA I L A B L E U P O N R E Q U ES T
PA G E 2
JOHN DOE
Street, City, State, Zip code
Tel: (123) 123-1432 | Email: sascrunch@example.com
P HARMA INC , New York, NY
Clinical SAS Programmer  Aug 2007-Dec 2010
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Leveraged industry expertise in providing topnotch SAS Programming and analysis support for phase III (oncology)
clinical trials
Served as primary SAS programmer and collaborate with statistician in analyzing initial data sets and generating
tables, listings and figures (TLFs) for clinical trials
Managed day to day technical operations such as creating tables and graphs to produce clinical study reports based
on collected requirement from the statisticians referring to the Statistical Analysis Plan (SAP)
Proactively performed and managed various duties such as data transformation and manipulation processes;
ORACLE database management; creating and modifying new and existing SAS programs; and producing Ad hoc
reports of various kinds like Listings, Tables, and Figures (TLGs/TLFs);
Led the development of SAS code for modeling data and directed the implementation of SAS/STAT procedures such
as Proc Lifetest, Proc lifereg, Proc Phreg, proc reg and Proc Glm for Survival analysis, logistic regression analysis
and other statistical analyses
Meticulously analyzed and validated data sets and SAS outputs with other programmers’ outputs and mockups in
SAP using PROC COMPARE, PROC CONTENTS, and PROC FREQ. Created formats for the coded data and used
PROC SQL for data validation
E DUCATIONAL B ACKGROUND
N EW YORK U NIVERSITY ,
Bachelor of Science in Statistics  Sept 2003-May 2007
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Design of Experiments and Regression  Clinical Trials  SAS Programming for Statistician
Categorical Data Analysis  Perspective in Advanced Biostatistics
R E F E R E N C E S AVA I L A B L E U P O N R E Q U ES T
PA G E 3