Clinical Data Analyst Position

13 hours ago

Kota, Rajasthan, India beBeeProgrammer Full time ₹ 15,00,000 - ₹ 20,00,000
Job Description

As a Senior Statistical Programmer, you will provide lead statistical programming support for multiple clinical projects using SAS. You will be responsible for delivering key regulatory-compliant output, developing programming documentation, writing efficient code, staying updated on programming techniques, and mentoring staff.

The ideal candidate will have a strong background in statistical programming with a focus on SAS. They will possess excellent analytical skills, the ability to process scientific and medical data, and strong communication skills.

  • Lead statistical programming support for multiple clinical research study projects or study teams.
  • Develop statistical programming methodologies using SAS (Base and Macros) and provide expert consultation to projects across the company.
  • Ensure 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.
  • Provide 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.
Qualifications
  • A bachelor's degree plus 4 years of 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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