- Lead statistical programming activities as Trial Programmer for phase I to IV clinical studies or assigned project-level activities. Co-ordinate activities of all programmers either internally or externally assigned to the study/project work. Make statistical programming recommendations at study level. Contribute to project level standards- Build and maintain effective working relationship with cross-functional teams, able to summarize and discuss status of deliverables and critical programming aspects (timelines, scope), e.g. as member of the Clinical Trial Team (CTT).- Review eCRF, discuss data structures and participate in data review activities.- Comply with company, department and industry standards (e.g. CDISC) and processes, review and develop programming specifications as part of the analysis plans.• Provide input into statistical programming solutions and/or ensure their efficient implementation. In consultation with the Statistician, responsible for development of programming specifications of analysis datasets and pooled datasets. Ensure timely and quality development and validation of datasets and outputs for CSRs, regulatory submissions/interactions, safety reports, publications or exploratory analyses (as required) in the assigned drug development study/project according to specifications- Responsible for quality control and audit readiness of all assigned statistical programming deliverables as well as accuracy and reliability of statistical analysis results.Maintain up-to-date knowledge of programming software (e.g. SAS) as well as industry requirements (e.g. CDISC SDTM/ADaM, eCTD, Define.xml), attend functional meetings and trainings.

Responsible for all Data Standard & Programming Activities of multiple studies. Working as a Project Lead for multiple studies.Development & Validation of SAS programs to create datasets as per CDISC- SDTM & ADaM standards and to generate TFL as specified in the protocol, statistical analysis plan (SAP) and mock shells. Preparation and Review of defne.xml, ADRG, SDRG.Developing & Validation of various documents to be submitted to Regulatory Agencies. Actively participation in Management activity

Work in a CRO as a Statistical Programmer-Write SAS program to create the analysis datasets, table, listing & figure, validation and review of clinical trial data- Creation of Tables and Listings as per the SAP and Mock shell provided.- Review Mock Shell and provide feedback.- Review Spec for SDTM and ADAM and provide feedback.- Creating SDTM and ADaM datasets as per the SPEC provided.- Create QC programs for Tables, Listings, SDTM and ADaM.- PEER review of the programs of team mates.- Update statistical macros as per the new requirement.- Validation of the statistical macros.- Worked a Study POC to communicate with Client.- Take part in study related calls\meeting.- Write and revise SOP’s as per need to maintain awareness and adherence to all current SOP’s.- Establish monitoring of data transfers for ongoing trials to identify data quality issues.

Currently working as a Senior Analyst in Analytics departtment of Eclerx Services Ltd.My Current role involves doing statistical analysis, Prediction Modelling ,Data Mining on a different domain for different clients using various tools like SAS,SPSS and R,Excel etc.

My role in WNS involves Analysis and implementations of campaigns which are being run in the US retail market.We basically decide the type of product to be offered to different segments of customers and measure the success/failure of the campaign over a certain period of time.Basically We manage the Campaign for a Different Retail base products.

Take a training on SAS modules.did different kind of projects like Finance related,market research etc