Data Science Lead

5 hours ago

Alwar, Rajasthan, India beBeeStatistical Full time ₹ 12,00,000 - ₹ 17,00,000
Senior Statistical Programmer Position

The Senior Statistical Programmer plays a key role in providing expert statistical programming support for multiple clinical projects using SAS. This includes delivering regulatory-compliant output, developing programming documentation, writing efficient code, and mentoring staff.

Key Responsibilities:

  • Leads statistical programming support for multiple clinical research study projects or study teams.
  • Develops statistical programming with SAS (Base and Macros) and provides consultation to projects across the company including statistical programming methodology.
  • Ensures sound methodologies are adopted by establishing proficiency of programming techniques required for clinical trials research which involve CDISC standards and analysis data sets or production of standard and custom tables listings and figures.
  • Provides key deliverables based on established profiency of regulatory requirements for clinical research E-submissions and/or study requirements for Sponsor, Regulatory, Investigator or Safety review meetings.
  • Develops programming documentation and annotations including specifications, review of mock shells, adhering to relevant Standard Operating Procedures and contributes to standardization efforts.
  • Writes well-documented, efficient, and high-quality code, conducts code review, supports cross-functional programming activities, and programming validation as needed.
  • Stays abreast of current statistical programming techniques to ensure adoption of sound methodologies.
  • Presents statistical programming topics internally and may present at external conferences.

Requirements:

  • A bachelor's degree plus 4 years Statistical programming experience as a CDISC/TLF Statistical programmer in Pharmaceutical/CRO environment, education in a scientific discipline preferred.
  • Understanding of GCP principles and other regulatory standards (e.g. 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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