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    Clinical SAS Sample Resume

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    genius_gks
    Srinivas A is a SAS programmer with Sristek Clinical Research solutions Pvt. Ltd in Hyderabad, India specializing in clinical trial programming using SAS 9.2. He has strong skills in SAS base procedures, macros, SQL, and statistical analysis. Some of his responsibilities include analyzing clinical trial data, generating tables and listings, finding data discrepancies, attending meetings, and creating reports. He has experience working on Phase II and Phase III clinical trials in therapeutic areas like psychology and hematology.

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    Clinical SAS Sample Resume

    Uploaded by

    genius_gks
    412 views2 pages
    Srinivas A is a SAS programmer with Sristek Clinical Research solutions Pvt. Ltd in Hyderabad, India specializing in clinical trial programming using SAS 9.2. He has strong skills in SAS base procedures, macros, SQL, and statistical analysis. Some of his responsibilities include analyzing clinical trial data, generating tables and listings, finding data discrepancies, attending meetings, and creating reports. He has experience working on Phase II and Phase III clinical trials in therapeutic areas like psychology and hematology.

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    A sample resume for Clinical SAS Programmers

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    Srinivas A is a SAS programmer with Sristek Clinical Research solutions Pvt. Ltd in Hyderabad, India specializing in clinical trial programming using SAS 9.2. He has strong skills in SAS base procedures, macros, SQL, and statistical analysis. Some of his responsibilities include analyzing clinical trial data, generating tables and listings, finding data discrepancies, attending meetings, and creating reports. He has experience working on Phase II and Phase III clinical trials in therapeutic areas like psychology and hematology.

    Copyright:

    © All Rights Reserved
    Download as PDF, TXT or read online from Scribd
    Download as pdf or txt
    412 views2 pages

    Clinical SAS Sample Resume

    Uploaded by

    genius_gks
    Srinivas A is a SAS programmer with Sristek Clinical Research solutions Pvt. Ltd in Hyderabad, India specializing in clinical trial programming using SAS 9.2. He has strong skills in SAS base procedures, macros, SQL, and statistical analysis. Some of his responsibilities include analyzing clinical trial data, generating tables and listings, finding data discrepancies, attending meetings, and creating reports. He has experience working on Phase II and Phase III clinical trials in therapeutic areas like psychology and hematology.

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    Srinivas.

    A
    SAS Programmer - Sristek Clinical Research solutions Pvt. Ltd
    Hyderabad, Andhra Pradesh - Email me on Indeed: indeed.com/r/Srinivas-A/c7092f88131f561c
    Proficient in Clinical Trial Programming using SAS 9.2 and Process in Pharmaceutical / CRO industry.
    Good programming experience with Base SAS with SAS Macro Language and SQL Procedures.
    Good Knowledge in SAS Base Procedures for reporting Tables, Listing and Graph like REPORT, FREQ,
    MEANS, UNIVARIATE, CHART & GCHART and PLOT & GPLOT.
    Good Knowledge in SAS Base Procedures for Data Processing Like FORMAT, SORT, TRANSPOSE,
    DATASETS, and SQL.
    Well versed with Statistical Analysis and Procedure used in SAS.
    Good Knowledge in Building SAS Macro programs for Clinical application.
    Good knowledge in SAS Base Procedure for Data Validation Prior and After Analysis Dataset like COMPARE,
    FREQ, MEANS, SQL and PRINT.
    Good Knowledge of Clinical Trial Management System (CTMS) & all phases (Phase I -IV) of clinical trial.
    Good Knowledge of 21 CFR Part 11, Good Clinical Data Management Practice (GCDMP)
    Knowledge in understanding SOP's.
    WORK EXPERIENCE
    SAS Programmer
    Sristek Clinical Research solutions Pvt. Ltd - Hyderabad, Andhra Pradesh - August 2011 to Present
    Sristek Clinical Research solutions Pvt. Ltd - Hyderabad (India)
    Project #1:
    PROJECT DETAILS:
    Therapeutic area: Psychology.
    Type of Study: Phase-II.
    Analysis: Demographic, Safety and Listings.
    Role: Programmer.
    Description:
    A Randomized, double-blind, Placebo-controlled and Multi-center trial to evaluate the Safety and Efficacy of
    the test drug with acute exacerbation of schizophrenia or schizoaffective disorder.
    The Study has four scheduled visits. That treatment duration is 7 weeks.
    Objective:
    To assess the efficacy of the study drug administered to subject with an acute exacerbation of schizoaffective
    disorder as measured by change from baseline to end of visit on the positive and negative syndrome scale
    total score.
    Responsibilities:
    Understanding the study documents like Protocol, Annotated CRF and SAP.
    Finding data discrepancies and send it to TL/PL.
    Attending the internal and project related meetings.
    Analyzing various tables using data manipulation techniques like merging, appending, concatenating and
    sorting.
    Creation of Baseline summary, Demographic, Safety and listings as per the SAP
    Generating the reports and send it for QC.
    Generating output files in the form of listing, HTML, RTF and PDF formats using SAS ODS.
    Coordinating with the team leader and the senior statistician.
    Project #2:
    PROJECT DETAILS:
    Therapeutic area: Hematology.
    Type of Study: Phase-III.
    Analysis: Demographic, Safety and Listings.
    Role: Programmer.
    Description:
    A randomized, open label, Multicenter study to evaluate the Efficacy, tolerability and Safety of the test drug
    as compared to reference drug in anemia associated with chronic kidney disease. The Study has 6 scheduled
    visits. That treatment duration is 24 weeks to 36 weeks.
    Objective:
    To study Efficacy and Safety of the study drug with respect to reference drug for correction of anemia and
    maintenance of hemoglobin associated with anemia in chronic kidney disease in dialysis patients.
    Responsibilities:
    Understanding the study documents like Protocol, Annotated CRF and SAP.
    Finding data discrepancies and send it to TL/PL.
    Attending the internal and project related meetings.
    Analyzing various tables using data manipulation techniques like merging, appending, concatenating and
    sorting.
    Creation of Baseline summary, Demographic, Safety and listings as per the SAP
    Generating the reports and send it for QC.
    Generating output files in the form of listing, HTML, RTF and PDF formats using SAS ODS.
    Coordinating with the team leader and the senior statistician.
    EDUCATION
    MCA
    Osmania University - Hyderabad, Andhra Pradesh
    June 2007 to June 2010
    ADDITIONAL INFORMATION
    TECHNICAL SKILLS:
    SAS System 9.2: SAS/ BASE, SAS Macro Language, SAS SQL Procedure and SAS/GRAPH
    Languages: SQL
    Office Packages: MS Office 2003 and 2007 (Word, Excel, PowerPoint)

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