Clinical SAS programmer Resume Princeton, NJÂ - Hire IT People

SUMMARY:

SAS Certified Professional with over 7+ years of experience in data analysis using Clinical SAS. Good Command in statistical analysis and research, data management, programming, robust knowledge of Base SAS, SAS/Macros, SAS/SQL.
Generating SDTM and ADaM datasets using SAS as per sponsor specifications..
Validating SDTM and ADaM datasets.
Generate tables of adverse event, demography, laboratory, vital sign, safety dataset, efficacy dataset, Medical history, concomitant medication, Disposition dataset.
Generation Listings of Adverse events, demography, laboratory, vital sign, safety dataset, efficacy dataset, Medical history, concomitant medication, Disposition dataset.
Generation of Summary and Shift Tables (Lab).
To perform the validation of tables and listings with parallel Programmer. Ability to work on multiple tasks and strong interpersonal, analytical and presentation skills.
Proficient with SAS/BASE, SAS/STAT, SAS/GRAPH, SAS/ODS, SAS MACROS and PROC SQL.
Working experience in preparation of CDISC SDTM datasets.
Good experience in Phase I to Phase IV Clinical Drug Trail studies. Understanding of clinical trial practices, procedures and methodologies.
Experience in producing reports, employing various SAS procedures like PROC SQL, PROC REPORT, PROC FORMAT, PROC FREQ, PROC MEANS and PROC UNIVARIATE, PROC SUMMARY.
Used base SAS procedures PROC FREQ, SQL, PROC SORT, Transpose and PROC MEANS to validate current results with expected results.
Experience in producing RTF, PDF, HTML files using SAS ODS facility.
Excellent programming skills in SQL and understanding of data management principles, such as joining data sets, data aggregation and sub - setting using PROC SQL.
Work collaboratively with statisticians and clinical data managers in analyzing the Clinical Trials and generating Reports.
Good communication skills, commitment, result oriented, hard working with a quest and zeal to learn new technologies. Highly organized and dedicated with a positive attitude and self-motivated. Good written, oral, and interpersonal communication skills.

TECHNICAL SKILLS:

SAS Tools: SAS Version 8/9, SAS-Base, SAS-Access, SAS-SQL, SAS-MACROS, SAS-GraphSAS-STAT, SAS-Report and SAS-ODS.:

Databases: Clinic-Trial, SQL server.

Data Visualization: Tableau 9.1(Desktop/Server)

Operating Systems: Windows

Languages: SAS, SAS Enterprise Guide.

Office Tools: MS OFFICE - Word, Excel, PowerPoint.

Core Competencies: Statistical programming, Clinical Trials, Data Analysis, Reports Development.

PROFESSIONAL EXPERIENCE:

Confidential, Princeton, NJ

Clinical SAS programmer

Responsibilities:

Understanding the statistical analysis plan and data management procedures (GCP&ICH Guide lines) using SOPs. Worked on SDTM and ADAM datasets development and validation.
Developing reports using Data step programming.
Reading data from various sources using Base SAS with related informats.
Generated Tables and Listings as per the mock shell. Generated Reports in Word document Format.
Worked on developed macros for SAS programs and tables Validation and Analysis and Report generation.
Validated/QC'ed other programmers output datasets before loading into final database.
Involved in creating transport files to move files between different environments.

Confidential, San Carlos, CA

Research Coordinator/Base SAS programmer

Responsibilities:

Leveraged industry expertise in providing top-notch 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.

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Clinical Sas Programmer Resume

Princeton, Nj

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