Expert Data Analyst

2 days ago

Vijayawada, Andhra Pradesh, India beBeeStatistical Full time ₹ 9,00,000 - ₹ 15,00,000
Job Description

The Senior Statistical Programmer role provides lead statistical programming support for multiple clinical projects utilizing SAS and offers expert consultation across the organization.

Key responsibilities include delivering regulatory-compliant output, developing programming documentation, writing efficient code, staying updated on programming techniques, and mentoring staff members.

Responsibilities

  • Provides lead statistical programming support for multiple clinical research study projects or study teams.
  • Develops statistical programming expertise with SAS (Base and Macros) and offers expert 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 either CDISC standards and analysis data sets or production of standard and custom tables listings and figures.
  • Delivers 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 may contribute 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 up-to-date with current statistical programming techniques to ensure the adoption of sound methodologies.
  • Presents statistical programming topics internally and may present at external conferences.

Qualifications

  • A bachelor's degree plus 4 years of statistical programming experience as a CDISC/TLF Statistical programmer in a Pharmaceutical/CRO environment, education in a scientific discipline is 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 is considered beneficial.

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