Description
SUMMARY * Certified Clinical SAS Programmer with years of experience in SAS Base/Advance with extensive knowledge in drug development process and clinical trials. * Extensively working on various therapeutic areas like Oncology, Dermatology, InfectiouDiseases, Respiratory, Copd, Immunology, Cardiovascular and Nuerology. * Extensively working on clinical trial projects (Phase I, II and III) with Bio-Statisticians, Data managers and Statistical programmers to create and analyze the clinical data, Tables, Figures, Listing (TFL), generate reports, graphs and create analysis datasets. * Extensively involved in data extraction and data cleaning according to the edit specifications and sas listing specifications documents. * Extensive knowledge of drug submission requirements, relevant ICH and FDA/EMEA guidelines, CDISC standards. * Proficient in creating analysis data sets with CDISC SDTM and ADaM standards. * Extensiveky working on open CDISC validator to review CDISC SDTM datasets. * Expertise in statistical SAS procedures and reporting procedures. * Expertise in producing RTF, PDF, HTML and MS Excel formatted files using SAS ODS facility. * Expertise in creating Macros and implementing SAS Macros to simplify programs flexibility to SAS program. * Excellent written, verbal, interpersonal communication and organization skills.
Work Experience
| COMPANY | POSITION HELD | DATES WORKED |
|---|---|---|
| (Confidential) | Project Manager & Business Analyst | 8/2016 - Present |
| Honeywell Inc. | Project Manager & Business Analyst | 4/2011 - 6/2016 |
| New York Stock Exchange | Sr. Techno Functional Analyst | 1/2011 - 4/2011 |
| Pfizer | Sr. Business Intelligence Analyst/Bi Manager | 11/2005 - 12/2010 |
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