Principal Computational Statistician

Eli Lilly
Location
US, Indianapolis IN
Job Type
Full-time
Posted
November 14, 2026
Salary Range
$69k - $196k USD

Job Description

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.


R&D Statistics - Scientist - R1

Summary

At the core, this R&D Statistics Scientist role applies statistics and data analysis to advance clinical study design, starting from rigorous sample size calculations and quantitative assessments. Working within Clinical Sciences, the role collaborates across functions to influence technical decisions and drive a culture of data-driven analytics, while contributing to the creation of formal technical reports and presentations that distill complex analyses for technical leaders and management. The work is executed under defined methods with close guidance, solving routine problems and delivering high-quality insights that inform study design and decision-making. Through clear communication and collaboration, the role helps elevate analytical standards and supports the team’s execution and learning.

Key Responsibilities

  • Conduct sample size calculations and quantitative assessments to support clinical study designs.
  • Collaborate with peers across functions to influence technical decisions and promote data-driven analytics.
  • Produce formal technical reports and presentations summarizing analyses for technical leaders and management.
  • Create and present technical documentation and analyses that inform local and network-level decisions.
  • Develop CDISC-compliant (ADaM/SDTM) submission-ready datasets, ensuring data integrity and regulatory alignment.
  • Design and execute statistical analysis plans to support clinical development and regulatory submissions.
  • Track and ensure compliance with evolving regulatory requirements affecting statistical analysis and data submissions.
  • Validate and ensure accuracy and consistency of statistical programming code and outputs for clinical submissions.

Core Capabilities

  • Apply defined methods to analyze clinical data and support study conclusions with clarity.
  • Use established statistical principles to perform routine analyses and interpret results for study design.
  • Present analyses and insights to technical leaders with clear, concise dialogue.
  • Manage own tasks and deadlines, seeking guidance when needed to ensure timely deliverables.
  • Adhere to applicable regulations and established procedures within routine analytical work.

Preferred Capabilities

  • Familiarity with scripting or basic automation to support data workflows.
  • Exposure to industry standards and analytical approaches guiding experiments.
  • Awareness of validation concepts applicable to computerized systems and data integrity.

Lilly is dedicated to helping individuals with disabilities to actively engage in the workforce, ensuring equal opportunities when vying for positions. If you require accommodation to submit a resume for a position at Lilly, please complete the accommodation request form (https://careers.lilly.com/us/en/workplace-accommodation) for further assistance. Please note this is for individuals to request an accommodation as part of the application process and any other correspondence will not receive a response.


Lilly is proud to be an EEO Employer and does not discriminate on the basis of age, race, color, religion, gender identity, sex, gender expression, sexual orientation, genetic information, ancestry, national origin, protected veteran status, disability, or any other legally protected status.

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.


R&D Statistics - Scientist - R1

Summary

At the core, this R&D Statistics Scientist role applies statistics and data analysis to advance clinical study design, starting from rigorous sample size calculations and quantitative assessments. Working within Clinical Sciences, the role collaborates across functions to influence technical decisions and drive a culture of data-driven analytics, while contributing to the creation of formal technical reports and presentations that distill complex analyses for technical leaders and management. The work is executed under defined methods with close guidance, solving routine problems and delivering high-quality insights that inform study design and decision-making. Through clear communication and collaboration, the role helps elevate analytical standards and supports the team’s execution and learning.

Key Responsibilities

  • Conduct sample size calculations and quantitative assessments to support clinical study designs.
  • Collaborate with peers across functions to influence technical decisions and promote data-driven analytics.
  • Produce formal technical reports and presentations summarizing analyses for technical leaders and management.
  • Create and present technical documentation and analyses that inform local and network-level decisions.
  • Develop CDISC-compliant (ADaM/SDTM) submission-ready datasets, ensuring data integrity and regulatory alignment.
  • Design and execute statistical analysis plans to support clinical development and regulatory submissions.
  • Track and ensure compliance with evolving regulatory requirements affecting statistical analysis and data submissions.
  • Validate and ensure accuracy and consistency of statistical programming code and outputs for clinical submissions.

Core Capabilities

  • Apply defined methods to analyze clinical data and support study conclusions with clarity.
  • Use established statistical principles to perform routine analyses and interpret results for study design.
  • Present analyses and insights to technical leaders with clear, concise dialogue.
  • Manage own tasks and deadlines, seeking guidance when needed to ensure timely deliverables.
  • Adhere to applicable regulations and established procedures within routine analytical work.

Preferred Capabilities

  • Familiarity with scripting or basic automation to support data workflows.
  • Exposure to industry standards and analytical approaches guiding experiments.
  • Awareness of validation concepts applicable to computerized systems and data integrity.

Lilly is dedicated to helping individuals with disabilities to actively engage in the workforce, ensuring equal opportunities when vying for positions. If you require accommodation to submit a resume for a position at Lilly, please complete the accommodation request form (https://careers.lilly.com/us/en/workplace-accommodation) for further assistance. Please note this is for individuals to request an accommodation as part of the application process and any other correspondence will not receive a response.


Lilly is proud to be an EEO Employer and does not discriminate on the basis of age, race, color, religion, gender identity, sex, gender expression, sexual orientation, genetic information, ancestry, national origin, protected veteran status, disability, or any other legally protected status.


Our employee resource groups (ERGs) offer strong support networks for their members and are open to all employees. Our current groups include: Africa, Middle East, Central Asia (AMECA), Black Employees at Lilly (BE@Lilly), Chinese Culture Network (CCN), EnAble, Evolve, Lilly Indian Network (LIN), Organization of Latinx at Lilly (OLA), Pride (LGBTQ+ Allies), Veterans Leadership Network (VLN) and Women’s Initiative for Leading at Lilly (WILL).


Actual compensation will depend on a candidate’s education, experience, skills, and geographic location.  The anticipated wage for this position is

$69,000 - $195,800

Full-time equivalent employees also will be eligible for a company bonus (depending, in part, on company and individual performance). In addition, Lilly offers a comprehensive benefit program to eligible employees, including eligibility to participate in a company-sponsored 401(k); pension; vacation benefits; eligibility for 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; and well-being benefits (e.g., employee assistance program, fitness benefits, and employee clubs and activities).Lilly reserves the right to amend, modify, or terminate its compensation and benefit programs in its sole discretion and Lilly’s compensation practices and guidelines will apply regarding the details of any promotion or transfer of Lilly employees.

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Frequently Asked Questions

Where is this job located, and is it remote, hybrid, or on-site?
The position is located in Indianapolis, Indiana, US, where Lilly is headquartered. The posting does not specify whether the role is remote, hybrid, or on-site.
What are the main responsibilities of this role?
Conducting sample size calculations and quantitative assessments for clinical study designs, designing and executing statistical analysis plans, developing CDISC-compliant (ADaM/SDTM) submission-ready datasets, validating statistical programming code and outputs, tracking regulatory compliance, and producing technical reports and presentations for leaders and management.
What qualifications or capabilities are expected?
Core capabilities include applying defined methods and established statistical principles to analyze clinical data, presenting insights clearly to technical leaders, managing your own tasks and deadlines, and following regulations and procedures. Preferred: scripting or basic automation skills, exposure to industry standards, and awareness of computerized system validation and data integrity concepts.
What is the salary range?
The anticipated wage is $69,000 to $195,800. Actual compensation depends on education, experience, skills, and geographic location. Full-time equivalent employees are also eligible for a company bonus based partly on company and individual performance.
What benefits does Lilly offer?
Eligible employees receive a company-sponsored 401(k), pension, and vacation benefits. Coverage includes medical, dental, vision, and prescription drug benefits, plus flexible spending accounts, life insurance and death benefits. Other benefits include time off and leave of absence benefits, and well-being programs such as an employee assistance program, fitness benefits, and employee clubs.
What team will I work in, and how much supervision is involved?
You will work within Clinical Sciences, collaborating across functions. The work is executed under defined methods with close guidance. You will solve routine problems and seek guidance when needed.
Can I request an accommodation during the application process?
Yes. If you need an accommodation to submit a resume, complete Lilly's accommodation request form at https://careers.lilly.com/us/en/workplace-accommodation. Other correspondence sent through that form will not receive a response.

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  • Verified H-1B salary data
  • Clinical-trial hiring momentum
  • Culture, benefits & locations
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Job Information

Source: workday
AI Relevance: 90/100 (Highly relevant)
Remote Type: onsite
Skills & Tags:
eli lilly pharma

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