Siva Pratap Reddy

1) Independently create, execute, maintain, and validate programs that transfer data across multiple data management systems or operating systems, combine data from a variety of sources and structures, generate and store summary data from a variety of sources, generate reports or combine multiple databases. 2) Independently create, execute, maintain, and validate programs that generate listings, tables and figures using SAS, or other appropriate languages. 3) Perform other programming tasks as necessary to support Clinical Data Management and Biostatistics. 4) Assess and ensure the validity of all program output. 5) Serve as a project lead and oversee work of other programmers on team. 6) Responsible for clearly documenting all work; managing assignments to meet timelines and producing high quality deliverables. 7) Function as a contributing member of a multi-disciplined team. 8) Actively seek information to gain good understanding of the role of the programmer in the overall process. 9) Increase knowledge base and professional skills in areas including programming, technology and techniques, clinical trials, and the pharmaceutical industry.

SAS Programmer in Biostats and Programming Department

Asst.SAS Programmer JOB FUNCTIONS/RESPONSIBILITIES: · Assists in the coding and execution of programs designed to produce analysis data sets, tables, figures and data listings as documented in the Statistical Analysis Plan. · Annotates listing and table shells based on analysis data set specifications,· Assists with tasks of setting up tracking spreadsheet and transcribing headers and footers to program input files. · Writes SAS programs to generate listings and replicate safety tables, · Notes data problems and discusses these, or any doubts about specifications, with project team, · Ensures accuracy of all output: Uses department quality checklist to review SAS code, log, and output, of programs written by self or by others in project team. · Reads all project team communications received as emails and attends project team meetings. Keeps informed of project status and issues. · Maintains of study documentation and files according to departmental policy. · Performs additional duties as assigned.

I have undergone Extensinve CYTEL internship program which includes following Real Time Projects: 1. Analysis Dataset Development • Role: Dataset Developer • Duration: 104 hours • Description: I have created macros to read file directory and based on required specification document (RSD) I have generated Analysis dataset using SAS Codes. 2. Analysis Dataset Validation • Role: Dataset validator • Duration: 44 hours • Description: In this project, I performed a role of independent analysis dataset validator. Here raw data, analysis datasets and RSD are given to me based on RSD using raw data I have developed analysis dataset and performed comparison study on it by writing PROC COMPARE and TRANSPOSE step in SAS. 3. Data Integration for PK Analysis • Role: Developed PK analysis dataset • Duration: 43 hours • Description: Here raw datasets provided from clinical lab and based on RSD I had created PK analysis dataset using SAS XPORT, LAG, MERGING statements. 4.Report generation • Role: Report developer • Duration:72 hours • Description: In this assignment analysis datasets, RSD, and mock shells were provided. I had generated report by writing independent sas codes. 5.Report validation • Role: Independent Report validator • Duration:40 hours • Description: In this project I was provided with RTF reports to be validate and analysis datasets from which RTF reports were created.I had validated these RTF reports and developers report datasets. 6.Graph Development • Role: Graph developer • Duration:80 hours • Description: I have generated percentage from baseline plot for a laboratory test and error bar graph for the pk end point.