Experience

IQVIA

• United States
• Hospitals and Health Care
• 700 & Above Employee

• Standards Engineer

  • Jan 2022 - Present



Centre for Human Drug Research

• Netherlands
• Research Services
• 200 - 300 Employee

• Senior programer

  • Oct 2018 - Nov 2021

  CDISC and Table listings CDISC and Table listings



Rosemind Consulting B.V.

• Netherlands
• Business Consulting and Services

• Sr. Standard programmer,CDISC centre of excellence

  • Oct 2016 - Aug 2018

  CDISC and DSUR CDISC and DSUR



IQVIA

• United States
• Hospitals and Health Care
• 700 & Above Employee

• Programmer,Analyst

  • Oct 2015 - Aug 2016

  ▪ Worked as a Team Lead were I am handling Phase3, Phase2 and Phase1 Trials.▪ Direct interaction with client on various issues related EDL\SDTM.▪ Perform extensive QC (Quality Check) and analysis in reviewing other team members work as well as render primary support and assistance in data validation and data cleaning in all phases of Clinical studies▪ Built study specific SDTM datasets.▪ Play a key role in developing, debugging, and validating the project-specific SAS programs to generate derived SAS datasets, summary tables, and data listings in accordance with departmental standards▪ SAS data transfer programming for converting the front-end data into SAS datasets as per SDTM standards.▪ Demonstrate proficiency in coordinating wide range of professional functions such as generating tables, listings, QC checking, and validating all outputs for Oncology clinical trials; developing reports for Safety and efficacy as per study requirements; debugging SAS compiling errors and identifying issues Show less

• Clinical Data Programmer

  • Jul 2013 - Sep 2015

  ▪ Done annotation on eCRF as per the company and SDTM standards.▪ Created the metadata for the trial.▪ Built study specific macros and tried to customize the process execution.▪ SAS data transfer programming for converting the front-end data into SAS datasets as per SDTM standards.▪ Experience in SAS edit-checks for validating the SAS datasets.▪ Tested and debugged SAS programs against the test data.▪ Processed the data in SAS for the given requirement using SAS programming concepts. Show less

• Associate Programmer

  • Jun 2011 - Jul 2013

  ▪ Overall management of creating specifications, SDTM Maplets, testing of Contivo Maps and deployment of the trial to CDR. ▪ Data extraction from clinical database using proc SQL.▪ Created specifications using Microsoft Excel for developing SDTM Maplets and SAS datasets.▪ Data cleaning and conversion into useful SAS Datasets and report generation.▪ Compared consistency of SAS variables, formats, and format codes. ▪ Data manipulation and edit-checks using SAS.▪ Created CDISC SDTM domain datasets from existing clinical trial data for Case Report Tabulation (CRT).▪ Quality Check (QC) through review, validation and testing of work done by peers. Show less



OneForce Solutions Pvt Ltd

• Software Development
• 1 - 100 Employee

• SAS consultant

  • Aug 2009 - Jun 2011

  ▪ Primary point-of-contact for the following: ▪ Team activities. ▪ Report generation as per client requirement. ▪ Maintenance of the existing report repository. ▪ Delivery of the daily business reports to the client. ▪ Import/Export of reports to/from Excel/SAS, SAS dataset generation and data manipulation using datasets. ▪ Extensive experience with SAS programming in the data step and with various SAS procedures in Base SAS, including thorough knowledge of SAS Macro. ▪ Importing and exporting data, presentation of data in elegant output using ODS systems like HTML, RTF, listing. ▪ Manipulating data using various base SAS procedure like proc append, merge, set, sort etc. ▪ Data cleaning and conversion into useful SAS Datasets and report generation. Show less