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    Sas Developer Resume

    Uploaded by

    Diku Shah
    This consultant has over 8 years of experience as a SAS developer with expertise in clinical trial data analysis, report generation, and regulatory submissions. They are proficient in SAS/Base, SAS/Stat, SAS/Access, SAS/Graphs and SAS/Macro and have worked on all phases of clinical trials. They also have experience writing SOPs, performing data validation, and leading teams as well as communicating with clients.

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    Sas Developer Resume

    Uploaded by

    Diku Shah
    140 views2 pages
    This consultant has over 8 years of experience as a SAS developer with expertise in clinical trial data analysis, report generation, and regulatory submissions. They are proficient in SAS/Base, SAS/Stat, SAS/Access, SAS/Graphs and SAS/Macro and have worked on all phases of clinical trials. They also have experience writing SOPs, performing data validation, and leading teams as well as communicating with clients.

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    Sample clinical SAS resume

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    sas developer resume

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    This consultant has over 8 years of experience as a SAS developer with expertise in clinical trial data analysis, report generation, and regulatory submissions. They are proficient in SAS/Base, SAS/Stat, SAS/Access, SAS/Graphs and SAS/Macro and have worked on all phases of clinical trials. They also have experience writing SOPs, performing data validation, and leading teams as well as communicating with clients.

    Copyright:

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

    Sas Developer Resume

    Uploaded by

    Diku Shah
    This consultant has over 8 years of experience as a SAS developer with expertise in clinical trial data analysis, report generation, and regulatory submissions. They are proficient in SAS/Base, SAS/Stat, SAS/Access, SAS/Graphs and SAS/Macro and have worked on all phases of clinical trials. They also have experience writing SOPs, performing data validation, and leading teams as well as communicating with clients.

    Copyright:

    © All Rights Reserved
    Download as TXT, PDF, TXT or read online from Scribd
    Download as txt, pdf, or txt
    of 2

    CONSULTANT NAME

    (SAS Developer)

    SUMMARY
    Certified SAS Programmer with over eight years of experience in Analysis, design,
    development, testing and validating the applications.
    Strong knowledge involving all phases (I-IV) of clinical trials.
    Worked on SAS/Base, SAS/Stat, SAS/Access, SAS/Graphs and SAS/Macro.
    Expertise in analyzing and coordinating clinical trial data, generating reports,
    tables, listings and graphs.
    Knowledge of CRF-Annotation with respect to various database designs.
    Knowledge of CRT Dataset creation from clinical trial data, CDISC and MedDRA for
    regulatory submissions.
    Reporting computer validation inspections in compliance with 21 Code of Federal
    Regulations (21 CFR, Part II).
    Optimized performance using Data Validation and Data cleaning on Clinical Trial
    data using Statistical procedures like PROC FREQ, PROC MEANS, and PROC UNIVARIATE.
    Involved in writing and updating Standard operating procedures (SOP) for reviews
    and approvals.
    Experience in Ad-hoc programming for clinical and data management departments.
    Knowledge of Programming languages such as C and UNIX SHELL.
    Highly motivated individual with excellent organizational and interpersonal skills.
    Possess strong ability to quickly adapt to new applications and platforms.
    Good team leader with strong analytical and communication skills.

    TECHNICAL SKILLS
    SAS Tools: SASV8, V9, SAS/BASE, SAS/ACCESS, SAS/SQL, SAS/MACROS, SAS/GRAPH,
    SAS/STAT, SAS/ODS.
    Databases: Oracle Clinical, Clin-Trial, SQL server, Oracle7x/8x.
    Operating Systems: UNIX, Linux, Windows98/2000/NT/XP.
    Languages: C/C++, Java, FORTRAN, Matlab, Perl.
    Office Tools: MS-OFFICE, Word, Excel, PowerPoint, FTP Tool.

    PROFESSIONAL EXPERIENCE
    Client Name From Date - To Date
    Statistical Programmer
    Project: Project Name
    Description:
    Responsibilities:
    Ability to write some common macros that are useful across multiple studies.
    Ability to work on multiple projects simultaneously and meet the deadlines as and
    when required.
    Perform validation on derived datasets and following the standard operating
    procedures during the validation process.
    Generate reports either in HTML, PDF or RTF formats according to the client
    specifications.
    Worked with Bio-statistician to analyze the results obtained from various
    statistical procedures like PROC ANOVA, GLM and mixed models.
    Extensive use of PROC SQL to perform queries, join tables.
    Conducted analysis and generated tables, listings and graphs using SAS.
    Used data _null_ and PROC REPORT to generate the outputs.
    Involved in helping out the new programmers initially with the i3 standards and
    project setups.
    Ability to deliver the TLG�s to the clients in the absence of the lead programmer
    and participating in off-site meetings.
    Active participation in monthly departmental meetings and providing the necessary
    inputs on how to improve the standards.
    Worked closely with Statisticians, Data managers.
    Extensive experience in working with people across other sites when required.
    Environment: SAS/Base, SAS/Stat, SAS/Graph, SAS/SQL, SAS/Macros, SAS/ Access, MS-
    Excel.

    Client Name From Date - To Date


    SAS Programmer/Analyst
    Project: Project Name
    Description:
    Responsibilities:
    Involved in Phase II and III clinical trials by providing required tables and
    listings.
    Developed routine SAS Macros to create tables, graphs and listings for inclusion in
    clinical study reports.
    Worked on time to event data to generate the required results for the comparator
    drug and the control drug.
    Reviewed large macro codes for running the programs.
    Worked on Kaplan-Meier macro to generate the graphs as per the requirements for FDA
    submission.
    Validating the data sets and comparing the results to that of source programmers
    output.
    Timely submissions on the ACM requests.
    Environment: SAS/Base, SAS/Stat, SAS/Graph, SAS/SQL, SAS/Macros, SAS/Access, MS-
    Excel.

    EDUCATION/CERTIFICATIONS/AWARDS
    M.S. in Biotechnology from Texas Tech University, USA
    SAS Certified Base Programmer V9

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