SAS programmer Resume

SUMMARY

7 years of experience as SAS programmer with strong emphasis in data analysis, Clinical trials and Health Care data.
Experience in Base SAS, SAS/Macros, SAS/SQL, SAS/Assist, SAS/Connect, SAS/STAT, SAS/Access, SAS/GRAPH, SAS/ETS, SAS ETL and SAS/ODS.
Strong expertise in design, development, analysis, testing and implementation of various SAS applications with in Clinical and Health care domains.
Posses excellent skills with PROC SQL, SAS DDE, SAS Arrays, SAS Base procedures, summary procedures and especially Data Step programming and reporting.
Good at creating, reviewing, retrieving, validating Datasets and to read, write, import and export to another data file formats.
Extraction and creation of data tables using SAS/Access, SAS/SQL from large scale databases.
Worked extensively on various SDTM domains such as Interventions - Exposure (EX), Comments (CM), Substance use (SU), Events - Adverse Events (AE), Medical History (MH), Disposition (DS), Clinical Events (CE), Protocol Deviation (DV), Findings - (EG), LB, IE, Vital signs (VS), Physical Examination (PE), Subject Characteristics (SC), PC, PP, Drug Accountability (DA).
Worked on Special Purpose Domains like Demographics (DM), Subject Elements (SE), Subject Visits (SV), Comments (CO) & their SUPPQUAL datasets.
Created summarize safety and efficacy (ISS/ISE) tables for FDA submission.
Preparing FDA E-submission ready reporting documentation including creating DDT’s, Transport files (XPORT format files).
Experienced in working closely with statisticians to provide SAS programming in analyzing clinical trials data and generating Statistical Analysis Files, Tables, Listings, Summaries, and Graphs.
Strong knowledge of Statistical Analysis Plan, Standard Operating Procedures, Protocols of clinical trials.
Experienced in data management and reporting.
Experience in producing external files and reports employing various SAS statements and procedures, such as null, ODS, Proc Print, Proc Report, Proc Tabulate in Clinical Trials.
Ability to work well within a team and with all levels of professionals.
Experience on SDTM Annotated CRF and Define.xml.
Experience in implementing CDISC SDTM for intervention, event and findings domain models and ADaM standards, knowledge of SDTM terminologies.

TECHNICAL SKILLS

SAS Tools: SAS V9.1.3, SAS V9.2, SAS V8.1 Base SAS, SAS/SQL, SAS/MACROS, SAS/STAT, SAS/GRAPH, SAS/ODS, SAS/ACCESS

Operating Systems: Windows 2003 Server, Windows NT/2000/XP, UNIX, Solaris

Databases: Oracle, MS SQL SERVER Oracle, & MS ACCESS

Internet Technologies: HTML, XML

Microsoft tools: MS office toolset(Word, Excel, Power point, Access)

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

Other: Lotus notes, ORIGIN Software

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