Description
Professional Summary: * SAS Certified Programmer with around 6 years of experience in clinical trials data analysis and reporting in Health care and Pharmaceutical fields. * Well-versed with clinical data analysis: analyzing clinical data, creating tables, listing and generating reports and graphs as per requirements, specifications and Statistical Analysis Plan (SAP). Experienced with SAS procedures such as Proc Format, Proc Freq, Proc Means, Proc Summary, Proc Univariate, Proc Report, Proc Transpose, Proc Sort, Proc Print, Proc Compare etc. Experienced with the use of SAS products including SAS/Base, SAS/Macro and SAS/ODS. * Familiar with CDISC SDTM models to generate standardized and compliant datasets from raw/ legacy data sets. * Experienced in creating SDTM and Analysis Datasets (ADaM) using SAP and CDISC Standards. * Well-versed with various clinical trial domains like Adverse Events (AE), Laboratory tests (LB), Exposure (EX), Vital Signs (VS) etc. * Performed documentation of all program files to maintain record for future reference * Outstanding organizational skills including ability to multi task and prioritize work to meet timelines and goals. * Effective team player with excellent, communication and interpersonal skills, ability to interact with colleagues across all disciplines and teams. Experienced with using SAS ODS to generate different file formats such as XML, RTF, PDF, and MS EXCEL. * Knowledgeable about different medical terminologies used in clinical trials and in development various software systems. * Extensive experience in working and analyzing databases, visualization of data using CDD (Collaborative Drug Discovery) Portal. Import/ export data from CDD.Analyzing research data using other statistical softwares such as PSAW (SPSS) and R language. Environment: SAS 9.4, SAS/Access, SAS/Base, SAS/Macro, SAS/Stat, SAS/ETL, SAS/Graph, SAS/SQL, Oracle, DB2, MS Office, UNIX and Windows. IOCB (Institute of Computational Biology) July 2009 - September 2010 SAS Programmer/Analyst Project: A Phase II studies of a combinational drug therapy pertaining to Oncology. Responsibilities: * Understanding of Study using SAP, Protocol and CRF and creation of Analysis datasets using client specifications. * Collaborated with the data management team to conduct quality check for raw data pertaining to SDTM programming. * Reported errors in table shell, analysis data, raw data and CRF to data management and clinics. * Worked on SDTM programming as per the CDISC standards for data sets such as AE, DM, VS, CM and LB. * Programming support for clinical trials phase I-II * Ensure adherence to SOPs Experienced with combining and stacking datasets and efficiently using DO loops, IF, IF ELSE, WHERE statements and arrays. * Extensively used SAS BASE procedures such as Proc Print, Proc Tabulate, Proc Report, Proc Summary, Proc Sql, Proc Means, Proc Freq, Proc Transpose, Proc Contents, and Proc Format etc. Environment: SAS 9.2/9.3, SAS/Access, SAS/Base, SAS/Macro, SAS/Stat, SAS/ETL, SAS/Graph, SAS/SQL, Oracle, DB2, MS Office, windows.
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