Experience

• 

  Pra health sciences

  Jun 2013 - May 2016

  Clinical programmer
• 

  Chiltern

  May 2016 - May 2017

  Programming analyst
• 

  Syneos health

  May 2017 - Aug 2018

  Statistical programmer ii
• 

  Parexel

  Aug 2018 - Aug 2023

  • Senior Principal Statistical Programmer

    Mar 2022 - Aug 2023

  • Principal Statistical Programmer

    Oct 2020 - Feb 2022

  • Senior Statistical Programmer

    Aug 2018 - Sept 2020
• 

  Iqvia india

  Sept 2023 - now

  Senior statistical programmer

  • Leading research efforts encompassing end-to-end activities involving aCRF, SDTM, ADaM, TFLs, and CRT package• Lead the development and validation of SAS (Statistical Analysis System) programs for data transformation, analysis, and reporting according to the SAP and regulatory requirements (e.g., FDA, PMDA)• Primary responsibility is to oversee and manage the statistical programming activities related to clinical trials• Analyzing and comprehending study requirements by reviewing the Study Protocol and CRF• Developing SDTM Define Ready Specification and corresponding Datasets• Extract, integrate, and manipulate data from various sources, including clinical databases and electronic case report forms (eCRFs), to prepare analysis datasets• Evaluating the SAP and mock shells to grasp the Analysis requirements• Formulating ADaM specification and generating ADaM datasets Show less