Senior Data Analyst and Programming Expert

2 days ago


Udaipur, Rajasthan, India beBeeStatistical Full time ₹ 15,00,000 - ₹ 17,50,000
Senior Statistical Programmer Role

Leverage your expertise in advanced SAS programming and proficiency in CDISC standards to support or lead Phase I-IV clinical trials. This is an exciting opportunity to drive innovation and patient treatment.

Job Responsibilities
  • Perform data manipulation, analysis, and reporting for clinical trial data, utilizing SAS programming.
  • Generate and validate SDTM and ADaM datasets/analysis files, tables, listings, and figures.
  • Produce high-quality QC/validation programming.
  • Generate complex ad-hoc reports from raw data.
  • Apply a strong understanding of efficacy analysis.
  • Create and review submission documents and eCRTs.
  • Communicate with internal cross-functional teams and clients for project specifications, status, issues, or inquiries.
  • Lead duties when called upon.
Requirements
  • A Bachelor's degree in Statistics, Computer Science, Mathematics, etc.
  • At least 7 years of SAS programming experience with clinical trial data in the pharmaceutical industry.
  • Study lead experience, preferably juggling multiple projects simultaneously.
  • Strong SAS data manipulation, analysis, and reporting skills.
  • Solid experience implementing CDISC SDTM / ADaM standards.
  • Good QC/validation skills.
  • Proficiency in efficacy analysis.
  • Familiarity with drug development life cycles and experience manipulating, analyzing, and reporting clinical trials' data.
  • Submissions experience using define.xml and other submission documents.
  • Experience supporting immunology, respiratory, or oncology studies would be beneficial.

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