Creating the Ad hoc reports using the SAS procedures and used ODS statements and PROC TEMPLATE to generate different output formats like HTML, PDF and excel to view them in the web browser.Validating and QC of the efficacy and safety tables.Developing the Macros at various instances for automating listings and graphing of clinical data for analysis. Using the Base SAS (MEANS, FREQ, SUMMARY, TABULATE, REPORT etc) and SAS/STAT procedures (REG, GLM, ANOVA, and UNIVARIATE etc.) for summarization, Cross-Tabulations and statistical analysis purposes.Involved in mapping, pooling and analysis of clinical study data for safety.Developing the SAS programs for listings & tables for data review & presentation including ad-hoc reports, CRTs as per CDISC, patients listing mapping of safety database and safety tables.Creating and deriving the datasets, listings and summary tables for Phase-I and Phase-II of clinical trials.Developing programs in SAS Base for converting the Oracle Data for a phase II study into SAS datasets using SQL Pass through facility and Libname facility.Extracting the data from various internal and external database (Oracle, DB2, Excel spreadsheets) using SAS/ACCESS, SAS/INPUT.Some of them include not necessarily all of them…. therapeutic areas a pharmaceutical company can work on and few of them include, anti-viral (HIV), Alzheimer’s, Respiratory, Oncology, Metabolic Disorders (Anti-Diabetic), Neurological, Cardiovascular. What is the therapeutic area you worked earlier?
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