Hi Friends,
Hope you are doing well.
I Have Clinical SAS Programmer Available immediately with me who is open to relocate all over US locations. So please do let me know if you have any Clinical SAS Programmer Positions. Feel Free to reach me at 734-956-4737*163 or Email me Vinod@addonusa.com.
Professional Summary:
· Experienced SAS Programmer with over 7 years of experience in working with SAS and SAS tools emphasizing on analysis, design, developing, testing and implementation of various projects for pharmaceutical and biotech industries on Windows and Unix environment.
· Extensive experience in BASE SAS, SAS/STAT, SAS/GRAPH, SAS/SQL, SAS MACROS, SAS/ACCESS, SAS ODS.
· Thorough knowledge in Statistical Analysis and advanced knowledge of statistical concepts like Regression analysis, Survival and Categorical Analysis, Sampling and Probability Theory & Repeated Analysis.
· Experienced in Base SAS procedures such as Proc Freq, Means, Summary, Univariate, Format, Import, Export, Report, Tabulate, Transpose, Datasets, Copy and Print.
· Experience with SAS/STAT procedures such as Proc Corr, Reg, Glm, Anova, Genmod, and Mixed.
· Hands on experience in Phase I, II, and III clinical data: analyzing clinical data, creating tables, listing and generating reports and graphs.
· Knowledge in preparing Integrated Summaries of Efficacy (ISE) and Safety (ISS) reports.
· Good working knowledge of clinical trials data like Demographic, Adverse Events (AE), Serious Adverse Events (SAE), Laboratory Data (LAB Data).
· Experience in using SAS to read, write, import and export to another data file formats, including delimited files, Spreadsheet, Microsoft Excel and Access tables.
· Worked with statisticians and clinical data managers to provide SAS programming in analyzing the data, generated reports, tables, listings and graphs.
· Familiar with ICH, GCP, FDA guidelines and Knowledge of industry practices with CDISC standards, electronic submissions standards and Models including SDTM, ADaM data models.·
· Familiar with Phase I, II and III of Clinical Trials during which worked closely with senior Bio-statisticians and clinical data managers to provide SAS programming in creating SAS datasets, analyzing the data, generated tables, figures (graphs) and listings (TFL).·
· Developed tables, graphs and listings for Clinical Study Reports by conducting, documenting and reporting in compliance with 21 Code of Federal Regulations (21CFR) Part 11, FDA and other regulatory compliances.·
· Exceptional problem solving skills for delivering useful and prudent solutions. A quick learner with an eye for detail and excellent analytical and quantitative skills.
· Good working knowledge of Clinical Trials data like Demographic data, Vital Signs, Adverse Events (AE), Serious Adverse Events (SAE), Laboratory data and Efficacy related data following CDISC standards.
· Excellent written and communication skills, self-starter and a good team player.
Technical Skills:
| Statistical Packages | SAS 8.2/9.1, SPSS 16, PASW 18, MS Excel, R, WEKA |
| SAS Tools | SAS/BASE, SAS/STAT, SAS/GRAPH, SAS/SQL, SAS/ACCESS, SAS/CONNECT, SAS/ODS, SAS/MACROS, SAS/Enterprise Guide |
| Database | Oracle, Microsoft SQL Server, SQL, MS-Access |
| Operating Systems | Windows 98/NT/XP/Vista/7, Unix |
Experience:
SAS Consultant & Analyst June 2011 – Present
Description: Kaiser Permanente is one of leading providers for Medical Insurance Plans in US. The project involved maintenance of existing Data Warehouse in correspondence to addition of revised business rules to data extracts and provide those extracts to business using ETL transformations, used as source data for many business applications as specified by business.
Responsibilities:
· Worked closely with the business users across different business Units to gather requirements for enhancing the existing process and functionality.
· Performed Data Analysis to understand the data from different source system.
· Analyzed various databases containing sales, titles, account, region etc data of the releases of various titles
· Developed Mappings between Source and Target and loaded the data and Validated Data for missing values and based on the requirements.
· Developed new or modified SAS programs and used SQL Pass Through and Libname methods to extract data from the Teradata DB.
· Cleaned existing data and converted them into useful SAS Datasets, merged datasets and created reports based on Ad-hoc requirements.
· Imported raw data files in excel format in SAS and subsequently created SAS Datasets and performed data manipulations on the datasets.
· Extensively used PROC SQL and MACROS with SELECT sub-queries to generate various reports by connecting to the Teradata DB.
· Used Dynamic Data Exchange (DDE) feature of SAS to transfer the data from and into SAS, MS Excel.
· Performed Data analysis, statistical analysis, generated reports, listings and graphs using SAS procedures such as Proc Means, Proc Tabulate, Proc Freq, and Proc Summary.
· Documented and presented data reports and model results to the team / manager.
· Used various Statistical Procedures like PROC FREQ, PROC REG, PROC ROBUSTREG, PROC ANOVA, and PROC GLM to analyze data and generate reports.
· Communicated with various personnel in the forecasting group and the statistical group for various requirement gathering and analysis of the data
Environment: SAS 8/9, SAS/BASE, SAS/MACROS, SAS/ACCESS, SAS/SQL, SAS ETL, SAS/ODS, Oracle9, Window NT/ 2000, UNIX, Teradata Excel/Access 2000, SAS/Enterprise Guide.
Sr.SAS Programmer Jan 2010 – June 2011
Description: Cancer Treatment Centers of America is a premier provider of cancer care. Their experts have been providing an unprecedented level of care to cancer patients at their hospital for more than two decades. Along with other services they offer Clinical Research, such as an ovarian cancer vaccine therapy for patients with recurrent and chemotherapy-resistant, late stage disease. The institute has conducted through more than 300 Clinical Trials, including one of the country's leading Phase I programs.
Responsibilities:
· Developed and maintained programs in SAS using SAS tools for Windows and UNIX.
· Worked on Phase I and Phase II clinical trials.
· Performed Validation and QC of datasets, tables, listing and graphs.
· Extensive experience with SAS programming in data step and with various SAS Procedures in Base SAS and SAS/Stat, including thorough knowledge of SAS Macro Language.
· Performed Data analysis, statistical analysis, generated reports, listings and graphs using SAS Tools–SAS/Base, SAS/Macros, SAS/Graph, SAS/SQL, SAS/Connect, and SAS/Access.
· Conducted statistical modeling for both continuous and categorical data, including linear and logistic regression, ANOVA, GLM and Mixed model.
· Extensively used SAS/ Macro facility to provide reusable programs that can be conveniently used time to time and, created tables, graphs and listing reports.
· Extensively used Data _Null, Univariate, Summary, Means, Freq and Chart procedures
· Produced quality customized reports by using PROC TABULATE, REPORT, and SUMMARY and also provided descriptive statistics using PROC Means, Freq, and Univariate.
· Prepared Integrated Summaries of Efficacy (ISE) and Safety (ISS) reports.
· Retrieved ORACLE tables with Proc SQL using 'Pass through Facility.'
· Formatted HTML, PDF and RTF reports, using SAS - output delivery system ODS.
· Designed and implemented statistical reporting processes for clinical data analysis.
· Involved in the submission of data in CDISC SDTM (V3.X).
Environment: SAS 8/9, SAS/BASE, SAS/MACROS, SAS/ACCESS, SAS/SQL, SAS/ODS, Oracle8, Window NT/ 2000, Excel/Access 2000 , SAS Enterprise Guide, MS Office, UNIX.
Sr. SAS Programmer Oct 2008 – Jan 2010
Description: Sanofi Aventis is the world's largest research-based biopharmaceutical company.
Responsibilities: ·
· Designed and implemented statistical reporting processes for clinical data analysis. Analyzed Phase I, II and III Clinical Trials.
· Developed and maintained programs in SAS using SAS tools for Windows in a user support environment.
· Extensive experience with the SAS programming and in data step and with various SAS Procedures in Base SAS and SAS/Stat, including thorough knowledge of SAS Macro Language.
· Programmed in SAS for analyzing data and producing tables and listings for safety and efficacy analysis in specified formats for submission or for other purposes.
· As a Programmer generated clinical data summary tables/Listings/graphs and reports using SAS.
· Interacted with Data managers, Statisticians and CRA's in clinical research and development by providing programming support for the processing of clinical data.
· As a Programmer I was involved in Phase II – III of the Clinical trials.
· Extensively used different Base SAS Procedures like Proc Sql, Proc Contents, Proc Print, Proc Sort, Proc Append etc.
· Extensively used different SAS/STAT Procedures like Proc Means, Proc Summary, Proc Univariate, Proc GLM etc.
· Extensively used PROC REPORT and PROC SQL Procedures.
· Programming with the use of Base SAS and SAS/MACROS.
· Involved in writing Test Plans ,Test cases and coordinating the Global Contacts; clarify the observed issues with global contact person and gives the any suggestions is required.
· Assist other staff in programming whenever required.
· To generate Efficacy Analysis Tables / Listings by using SAS Programming.
· Generate Safety Analysis Tables / Listings through Sanofi Aventis standard tool.
Environment: SAS/BASE, SAS/MACRO, SAS/SQL, SAS/GRAPH, SAS/IMPORT SAS/EXPORT, SAS/STAT, SAS/ACCESS, SAS/ODS, SQL Server, Windows.
SAS Analyst Aug 2007 – Oct 2008
Description: Assurant Health is part of Assurant, a premier provider of specialized insurance products and related services in North America and selected international markets.
Responsibilities:
· Worked on writing, editing, validating and debugging code in BASE SAS and MACROS.
· Extensively used PROC REPORT for detailed reports.
· Assisted seniors and follow programmers in validation, edit checks and data review listings.
· Used SAS /ACCESS to gather data from RDBMS like ORACLE.
· Worked in multidisciplinary teams closely with statisticians, medical writers and data managers.
· Compiled raw data and created datasets for all programs.
· Developed SAS macros for data cleaning and reporting.
· Assisted in checking and quality assurance of all programming code and datasets.
· Programming of data listings using SAS tools.
· Created and extracted Oracle tables from SAS and within Oracle by using SAS/Access, SAS/SQL, and DBLOAD.
· Prepared analysis plans including specifications for table listings. Taking raw data and creating datasets.
· Used SAS for pre-processing data, data analysis, generating reports, and statistical analyses for marketing and financial decisions.
· Creating permanent formatted SAS data sets and developed reports using PROC REPORT, PROC TABULATE and DATA_NULL_ for analysis.
· Wrote Edit check programs and listings of data.
· Ran weekly and monthly reports using SAS.
Environment: SAS/BASE, SAS/ACCESS, SAS/SQL, MS Project, Windows NT/2000, Crystal Reports
SAS Programmer Aug 2006 – June 2007
Description: Varda Biotech is a technology based and knowledge driven enterprise, offering integrated services in Biotechnology and Pharmaceuticals. It offers Clinical Developmental Services in areas such as Bioequivalence, Clinical trials related activities, Data Management and Biostatistics Operations. Clinical Research Services are provided to Pharmaceutical Industries and Clinical Research oriented companies that are interested in Clinical Research based on ICH guidelines and International companies interested in using India as a base for their biometric operations. The information, collected as CRF (Case Report Form or Clinical Report Form) would be entered as data entries and sent to us as raw clinical data. The project involved statistical analysis of Phase II – Phase IV Clinical Trials data extraction, analyzing and reporting.
Responsible for analyzing data received; involving in Data Manipulation and Validation; writing and developing SAS reports to display results; performing integrated summaries and electronic submission activities.
Responsibilities:
· Responsible for developing new SAS programs and modifying existing SAS programs.
· Heavily involved in data Manipulation and validation·
· Convert MS-Excel, MS-Access database and dbase tables into SAS data sets.
· Created analysis data sets from raw data sets.
· Involved in clinical trials programming of data tables and listings for reporting on safety and efficacy.
· Produced quality customized reports by using PROC REPORT, PROC TABULATE and PROC SUMMARY.
· Provided descriptive statistics using PROC MEANS, FREQ and UNIVARIATE.
· Provided statistical SAS programming for biostatistics and data management deliverables that support both in-house clinical (or pre-clinical) studies and prospective, ongoing clinical trials per GCP and ICH standards/regulations.
· Generated Graphs using PROC GPLOT AND GCHART and SAS Graphics Editor.
Environment: SAS 6.0, SAS/Base, SAS/Graph, Proc Transpose, Proc Summary, Proc Tabulate, Proc Report, SAS/Stat, Excel, Access, Oracle, Win NT
Junior SAS Clinical Analyst Apr 2005 – Aug 2006
Description: Reddy's Labs is a leading research-based pharmaceutical company with a broad pharmaceutical product line and wide variety of vaccine products, over-the-counter (OTC) medicines, oral care products and nutritional healthcare drinks. As a SAS analyst, performed relevant statistical analysis of surveys and economic data, captured during clinical trials and performed quality control (QC) checks against database to ensure correct data was entered.
Responsibilities:
· Created database conversion programs for clinical studies according to the Data Management Plan (DMP), tracked each receipt of non-CRF data, assisted in the process of locking & freezing databases, sent interim, frozen and final databases to client.
· Responsible for data collection, management and manipulation of clinical trials database for Phase 1 clinical trials.
· Performed statistical analysis including testing SAS code for Phase 1 clinical trials.
· Created standardized datasets from the existing datasets.
· Created and modified SAS macros.
· Involved in CRF review and quality check.
· Compared consistency of SAS variables, formats, and format codes across multiple studies.
· Performed Validation checks for accuracy and integrity of clinical data.
· Created Summary Reports and Tabular Reports using Proc Report and Proc Tabulate.
Environment: BASE SAS, SAS Macros, SAS/Access, Windows, MS-Access, Proc Reports
Education:
· Professional Science Masters, MI, USA
· Bachelor of Technology, Biotechnology, JNTU, India
Vinod
ADDON Technologies, Inc.
Direct: 734-956-4737 Ext - 163
Fax: 734-418-2603
Mail ID: vinod@addonusa.com
URL: www.addonusa.com
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