SAS programmer Resume

SUMMARY

Having 6+ years of work experience using SAS, SAS/Macros and SQL; general SAS programmer with Clinical, Health care & Pharmaceutical background.
Thorough knowledge of Clinical Trials data like Demographic data, Vital Signs, Adverse Events (AE), Medical History, Diagnosis, Laboratory data and other Safety and Efficacy related data. Have knowledge about Health care data like Inpatients, Outpatients, Service, etc.
Experience working in the Clinical Research field.
Broad Knowledge of Life Sciences with extensive experience in the clinical trial process (Phase I - IV).
Generating Safety and Efficacy tables, data listings and graphs.
Design and review CRF and data validation directives for a clean and accurate database.
Knowledge in creating datasets and table programming for ISE (Integrated Summary of Efficacy) and ISS (Integrated Summary of Safety) submissions to the FDA and EMEA.
Extensively involved with verification and validation of reports based on company specific SOPs and 21CFR Part 11 code of federal regulations for electronic submission.
Expertise in collaboration with other SAS programmers/biostatisticians to create derived datasets, display, summarize and analyze data for clinical trials, and QC the results.
Extensive experience in SAS/BASE, SAS/MACRO, SAS/STAT, SAS/GRAPH, SAS/ACCESS, SAS/ODS, SAS PC (V 8/8.2/9.1.3/9.2 ), SAS/SQL.
Performed Cleaning Techniques, QC Validation and Edit Checks as per protocol designs on Clinical Data.
Have advanced knowledge in SAS programing, especially use of complicated Macros and PROC SQL connecting to various RDBMS, flat files, etc.
Analyze functional problems and make recommendations for enhancements or modifications to deliver solutions.
Familiarity with ICH, GCP guidelines and Electronic Submission standards.
Knowledge of industry practices with CDISC standards, SDTM and ADaM.
Worked closely with Statisticians, Data managers and Medical writers.
Capable of modifying or enhancing applications in accordance with business requirements in a time frame appropriate to meet the needs of a Production environment
Proficient with the Microsoft Office Suite of applications and possess the capability of producing professional-looking documentation, flowcharts, and proposals.
Excellent communication and writing skills, patience, professionalism and ability to effectively interact with staff and management alike.

TECHNICAL SKILLS

Statistical Software: SAS v7.1/8.0/9.1, SAS/BASE, SAS/STAT, SAS/SQL, SAS/MACRO, SAS/GRAPH, SAS/ACCESS, SAS/ODS, Enterprise Guide

Databases: Oracle Clinical, MS Access, Teradata, DB2

Operating Systems: Windows 9x/2000, XP, NT, UNIX

Software’s: MS Word, MS Excel, VISIO, MS Access, MS PowerPoint

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