ClinChoice

Statistical Programmer/Analyst III - 2

ClinChoice · Bangalore, India
Bangalore, India Closed
Applications are closed for this role. It was originally posted 2026-07-01. It’s no longer accepting applicants — see roles ClinChoice is still hiring for →, or browse the live openings below.
Type
Full-time
Experience
2+ yr

Responsibilities:

  • Analyze data and report statistical results.
  • Develop SDTM specifications for programming datasets following CDISC standard.
  • Independently develop SAS programs to create SDTM datasets.
  • Develop ADaM analysis data specifications for programming following CDISC standard with minimum supervision.
  • Independently develop SAS programs to create ADaM datasets for Analysis and Reporting based on Statistical Analysis Plan.
  • Develop, debug, and maintain SAS programs and macros to create Tables, Listings and Graphs for Clinical Study Report following CDISC, industry guidelines and Statistical Analysis Plan.
  • Independently implement SAS programs to generate Define-XML package for FDA submission.
  • Develop SAS programmable edit checks to assist data monitoring, document and report data issue to Data Management.
  • Implement statistical data analysis and communicate with statisticians for statistical input.
  • Support regulatory electronic submissions to Food and Drug Administration (FDA) and other worldwide regulatory authorities.
  • Perform other programming tasks as needed per management requests.

Skills and Qualifications:

  • Bachelor’s/Master’s degree in Statistics, Mathematics, Computer Science, Electrical Engineering, Biotechnology or related scientific disciplines with 2+ years of statistical programming experience required.
  • Proven knowledge and training in high level computing languages such as SAS, C/C++, Java, R, Python, MATLAB and SQL. Database programming experience is a plus.
  • Ability to translate statistical analysis plan into SAS programming language, to update and fix existing programs.
  • Working knowledge of Good Clinical Practices, Clinical research, Clinical trial process and related regulatory requirements and terminology.
  • Good understanding of clinical drug development process.
  • Team player, strong communication skills and coordination skills.
  • Detail oriented and ability to learn and adapt to changes.
  • Proficient in Microsoft Office Suite, e.g., Word, Excel, PowerPoint, etc.
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