Deena Marpu

Biography

I have 6 years of experience in Clinical SAS programming. I have worked on multiple Indications and multiple Therapeutic Areas.I have extensively worked on different regulatory (FDA, PMDA, EMEA) submission activities like CSPD specification preparation, SCS, SCE, HAQs, and CRTs. Good Knowledge of SAS Programming & Biostatistics which includes Sample size Calculation Using SAS,Randomization Schedule,Statistical Analysis plan for Clinical Trails,Various Parametric & Non Parametric Bio-Statistical tests like t-test,ANOVA,ANCOVA, Chi-square,F-Test,Sign Test,Confidence Intervals. Application of Statistics in Design of Experiments(DOE) according to ICH Q8 Guide lines. Additionally I have worked on the full cycle of Clinical Data Analysis and Reporting Automation Tool (i.e. User requirement specification, Development, Validation). I have also worked on many standardization projects like ADaM metadata repository, LSH setup.

Research Interest

 Clinical Trials  SAS Pharmaceuticals