Computational Statistician (R2-R4)

LillyIndianapolis, IN
$46,842 - $134,835Hybrid

About The Position

At Lilly, the work is demanding because patients are waiting. We unite caring with discovery to help make life better for people around the world, knowing that every decision, every detail, and every day matters. Headquartered in Indianapolis, Indiana, our over 50,000 employees around the globe take on complex challenges to discover and deliver life-changing medicines, strengthen how health is understood and managed, and support the communities we serve. This is hard, urgent, selfless work—but it’s work worth doing. If you’re driven by purpose and ready to bring your best to work that truly matters for patients, we invite you to join us. Eli Lilly and Company seeks a Computational Statistician (R2-R4) to develop data analysis plans for clinical trials. Assist in selecting statistical methods for data analysis. Conduct peer reviews of work products from statistical colleagues. Establish reporting databases and analyze clinical trial data by working with clinical research associates and project statisticians. Implement previously outlined statistical analysis plans. Ensure accuracy of reported data and statistical analyses by applying relevant disease states and competitive landscapes.

Requirements

  • Master’s degree in Biostatistics, Statistics, Computer Science, or related a STEM field
  • 1.5 years of academic or employment experience with implementing statistical analyses and reporting in clinical trials
  • Minimum of 1.5 years of experience with statistical programming/visualization software, including SAS, R, and Spotfire
  • Minimum of 1.5 years of experience writing and executing SAS macros and R functions
  • Minimum of 1.5 years of experience with investigating raw data issues identified during statistical analysis
  • Minimum of 1.5 years of experience with developing and validating SDTM and ADaM specifications and datasets in compliance with CDISC standards

Responsibilities

  • Develop data analysis plans for clinical trials.
  • Assist in selecting statistical methods for data analysis.
  • Conduct peer reviews of work products from statistical colleagues.
  • Establish reporting databases and analyze clinical trial data by working with clinical research associates and project statisticians.
  • Implement previously outlined statistical analysis plans.
  • Ensure accuracy of reported data and statistical analyses by applying relevant disease states and competitive landscapes.

Benefits

  • Telecommuting benefit available
  • company bonus (depending, in part, on company and individual performance)
  • company-sponsored 401(k)
  • pension
  • vacation benefits
  • medical, dental, vision and prescription drug benefits
  • flexible benefits (e.g., healthcare and/or dependent day care flexible spending accounts)
  • life insurance and death benefits
  • certain time off and leave of absence benefits
  • well-being benefits (e.g., employee assistance program, fitness benefits, and employee clubs and activities)
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