Senior Quantitative Analyst

11 hours ago


Nashik, Maharashtra, India beBeeStatistical Full time ₹ 1,38,24,000 - ₹ 2,01,60,000

Sponsored by a leading pharmaceutical client, you will work as a Senior Statistical Programmer within a global team.

This role can be performed remotely and offers the opportunity to work on Phase I-IV clinical trials with advanced SAS programming skills and proficiency in CDISC standards.

Key Responsibilities:
  • Data manipulation, analysis, and reporting using SAS programming
  • Generating and validating SDTM and ADaM datasets/analysis files, and tables, listings, and figures
  • Production and QC/validation programming
  • Generating complex ad-hoc reports using raw data
  • Efficacy analysis
  • Creating and reviewing submission documents and eCRTs
  • Communicating with internal teams and clients for project specifications, status, issues, or inquiries
Requirements:
  • Bachelor's degree in Statistics, Computer Science, Mathematics, etc.
  • At least 7 years of SAS programming experience with clinical trial data in the Pharmaceutical & Biotech industry
  • Study lead experience, preferably juggling multiple projects simultaneously
  • SAS data manipulation, analysis, and reporting skills
  • CDISC SDTM / ADaM standards implementation
  • QC/validation skills
  • Ad-hoc reporting skills
  • Efficacy analysis proficiency
  • Drug development life cycle experience and clinical trials' data manipulation, analysis, and reporting
  • Submissions experience using define.xml and other submission documents
Benefits:
  • Opportunity to work with autonomy and ownership
  • Collaborative cross-cultural environment
  • Flexible remote work arrangement

We are looking for a highly skilled and experienced Senior Statistical Programmer to join our team. If you have a strong background in SAS programming and a passion for working on complex clinical trials, we encourage you to apply.



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