Clinical Sas Programmer
Current• Thorough knowledge in SAS Programming, merging SAS Data Sets, Macro Facility, Preparing Data, PROCs, Producing Reports, SAS, SAS Formats, SAS Functions, Storing and Managing Data in SAS Files.• Developed programs to generate tables and supporting Listings, Integrated Safety Reporting, and Electronic Submissions to Regulatory authorities. • Worked with Data Managers to ensure Data Integrity did Data Cleaning and data Validation and produced TLGs as per the requirement of the Clinical and Data Management Department (DMD).• Provided statistical programming expertise in the production of Reports, CRTs (Case Report Tabulation/Analysis Datasets), Graphics, Summaries, and Listings from clinical trial data.• Participated in documentation and data program archiving.• Contributed to the preparation of Statistical Analysis Plans. Prepared, documented, and tested required programs and procedure data displays efficiently for inclusion in integrated clinical statistical reports and other similar reports. • Created CRT Datasets used for FDA Submissions. • Good working knowledge of CDISC standards like STDM, and ADAM.• Worked closely with Data Management Group to create data cleaning and data validation listings. • Performed QC, Data Validation and Edit Checks using various procedures and Macro facility.