ONYX PHARMACEUTICALS CA: * My recent project with onyx pharmaceuticals, And role was clinical sas program mer

for clinical study data phase I to Phase II. * Study was double blinded and randomly distributed therapeutic area was oncolog y especially for the patients who * Suffering with liver carcinoma and kidney failure, to compare and contrast wit h existing drug. * Defined baseline measurements and find that base line changes for each and eve ry treatment cycle. And calculated percentage changes, data compared statistical ly before and after drug intervention. * I have Analyzed and written the code According to protocol and system specific ation. * Executed and validated SAS program As defined in the SAP. * Fallowing the rules and regulation as defined in the SAP and created new analy sis datasets, variable, * Listing ,graphs and summery tables. And then used different bas/sas Sas/stat p rocedures Analyze the clinical trial data statistically. * Implemented SAS data management techniques data to manipulation,pooling,analys is data for required output. * Collaborated with statistician, medical writers to get accurate information re garding data issues. * Generated reports such as ISS and ISE as defined in the report analysis plan. * Implemented CDISC standards by using ProcCDISC for safety and efficacy analysi s. ACCESS PHARMACEUTICALS TEXAS: * During this project worked as sas programmer, where combination drug developed for the Treating the patients who are suffering cancer and treated surgically s tage III colon cancer. * The investigational drug compares and contrasts with existing drug. * Extracted data from oracle using SQL pass through facility and Libname stateme nt, for clinical study data phase II and III. * Use several input formats, labels and data management techniques to process ra w data into sas. and then sorting merging calculating values for desired out put as defined in the report analysis plan. * written the macro code for when the code required several time such as %macro sort,%macroproc. etc. * Created graphs and Keplan Mayer survival estimates during time to event analys is using procgplot,proc Gchart proc lifetest,etc. * Joined the table for merging Adverse event medication and concomitant medicati on for the medication records by using proc sql as many to many merge. And listi ng the demographic data using proc report and data_null_statement. * Involved in creation summery tables of Demographic, AE,concomitant medication * Experienced quality control methods error traping,using debug option,contional statements for logical expression and validation data according to SAP. GENZYME PHARMACEUTICALS: * Genzyme pharmaceuticals is developing innovative products(antiviral, Antibacte rial) for treating patients suffering with * Battle infections effected on digestive, respiratory, urinary systems. The stu dy was phase I to III double blinded randomly distributed. Analysis clinical stu dy data for safety and efficasy analysis. * Cross check the data against CRF (case report form) * Used and created new macros for analyzing and creating automate tables listing and graphs. * performed statistical analysis for clinical study by SAS/STAT BASE/SAS procedu

res * such as proc corr ,proc reg. etc proc freq,proc univariate proc ttest one samp le ttest, two sample ttest, * Analysis datasets and statistical reported created according to statistical an alysis plan system required plan. * created Graphs and keplan mayer survival estimation, time to event analysis by using Proc gplot proc lifetest proc gchart, etc. * Created ODS format files PDF,HTML, RTF by using output delivery system(ODS). * validate the sas program variables and listings, with validator program using proc compare. Clinical SAS project description