Senior Data Scientist

1 day ago

Belgaum, Karnataka, India beBeeStatistical Full time ₹ 15,00,000 - ₹ 18,00,000
Job Overview

The Senior Statistical Programmer spearheads statistical programming support for multiple clinical projects, utilizing SAS and providing expert consultation across the industry. Key responsibilities include delivering regulatory-compliant output, developing programming documentation, writing efficient code, staying updated on programming techniques, and mentoring staff.

Key Responsibilities
  • Provides lead statistical programming support for multiple clinical research study projects or study teams.
  • Develops statistical programming with SAS (Base and Macros) and provides expert consultation to projects across the industry including statistical programming methodology.
  • Ensures sound methodologies are adopted by establishing proficiency of programming techniques required for clinical trials research involving CDISC standards and analysis data sets or production of standard and custom tables listings and figures.
  • Presents key deliverables based on established proficiency of regulatory requirements for clinical research E-submissions and/or study requirements for Sponsor, Regulatory, Investigator, or Safety review meetings.
  • Writes well-documented, efficient, and high-quality code, conducts code review, supports cross-functional programming activities, and programming validation as needed.
Requirements
  • A bachelor's degree plus 4 years of experience in statistical programming as a CDISC/TLF Statistical programmer in a Pharmaceutical/CRO environment, education in a scientific discipline preferred.
  • Understanding of GCP principles and other regulatory standards such as FDA, EMA, and ICH guidance and recommendations in Clinical Research.
  • Good analytical skills with the ability to process scientific and medical data.
  • Strong statistical programming skills in SAS, familiarity with R, Python, or other relevant statistical software considered beneficial.

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