Advanced Statistical Programmer

13 hours ago


Davangere, Karnataka, India beBeeStatistical Full time US$ 1,20,000 - US$ 1,50,000
Advanced Statistical Programmer Role Overview

This senior-level position involves leveraging advanced SAS programming skills and CDISC standards to support or lead clinical trials.

The ideal candidate will be able to work independently and collaboratively as part of a globally dispersed team environment.

  • Key Responsibilities:
  • Perform data manipulation, analysis, and reporting of clinical trial data using SAS programming
  • Generate and validate SDTM and ADaM datasets/analysis files and tables, listings, and figures
  • Develop production and QC/validation programming
  • Generate complex ad-hoc reports using raw data
  • Apply strong understanding/experience of efficacy analysis
  • Create and review submission documents and eCRTs
  • Communicate with internal cross-functional teams and clients for project specifications, status, issues, or inquiries
  • Lead duties when called upon

Qualifications:

  • Bachelor's degree in Statistics, Computer Science, Mathematics, etc.
  • At least 7 years of SAS programming experience working with clinical trial data in the pharmaceutical industry
  • Study lead experience, preferably managing multiple projects simultaneously
  • Strong SAS data manipulation, analysis, and reporting skills
  • Solid experience implementing the latest CDISC SDTM / ADaM standards
  • Strong QC/validation skills
  • Good ad-hoc reporting skills
  • Proficiency in efficacy analysis
  • Familiarity with drug development life cycle and experience with manipulating, analyzing, and reporting clinical trials' data
  • Submissions experience utilizing define.xml and other submission documents


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