Senior Statistical Programming Lead

2 weeks ago


Bengaluru, Karnataka, India IQVIA Full time
About the Role

We are seeking a highly skilled Senior Statistical Programmer to join our team at IQVIA. As a key member of our clinical research team, you will be responsible for designing, developing, and implementing statistical programming solutions for our clients.

Key Responsibilities
  • Develop and maintain SAS programming specifications, datasets, and TLFs
  • Conduct plausibility and completeness checks of programming output across each study
  • Lead and own identified opportunities for process improvement
  • Identify, build, and validate SAS Macros
  • Contribute to activities in validation and implementation including Standard Reporting Systems, SAS macro utility programs, and associated tools
Requirements
  • More than 5+ years of experience in Statistical Programming in the pharmaceutical or medical devices industry
  • Excellent knowledge of SAS Base, good knowledge of SAS Graph, and SAS Macros
  • Strong understanding of CDISC standards (SDTM and ADaM), relational database components, and theory
  • Excellent application development skills and strong understanding of clinical trial data
  • Good understanding of ICH E6, ICH E3, ICH E8, ICH E9, and clinical research processes
Preferred Qualifications
  • Good verbal and written communication skills
  • Ability to work on multiple projects, plan, organize, and prioritize activities
About IQVIA

IQVIA is a leading global provider of advanced analytics, technology solutions, and clinical research services to the life sciences industry. We believe in pushing the boundaries of human science and data science to make the biggest impact possible – to help our customers create a healthier world.



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