PhD Statistics – Intern to Fulltime

Eli Lilly and Company

Applications Closed

Posted 23 days ago

Internship

Indianapolis, Indiana

In Person

Smart Summary

The Clinical Project Statistician develops or assists in developing protocol designs, clinical plans, and data analysis plans in collaboration with medical colleagues. Responsibilities include selecting statistical analysis procedures, analyzing data for clinical studies, and authoring relevant sections of protocols and statistical analysis plans.

This role is ideal for PhD students in Statistics or Biostatistics who have completed a Lilly internship and are expected to graduate by August 2026. The position involves statistical trial design and analysis, collaboration on study protocols, and communication of results, requiring proficiency in statistical programming languages and strong interpersonal skills. This role offers the opportunity to transition from an intern to a full-time employee.

Must Have Skills for ATS

Statistical Trial Design

Data Analysis

Protocol Design

Statistical Methods

Data Quality Assurance

Novel Statistical Methodology

Peer-Review

Communication Of Results

Regulatory Submissions

Therapeutic Area Knowledge

Regulatory Compliance

Innovative Methodology

Causal Inference

Machine Learning

Bayesian Statistics

Adaptive Designs

Job Description

At Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our employees around the world work to discover and bring life-changing medicines to those who need them, improve the understanding and management of disease, and give back to our communities through philanthropy and volunteerism. We give our best effort to our work, and we put people first. We’re looking for people who are determined to make life better for people around the world.

Functional Overview & Responsibilities  

Our Global Statistical Sciences department includes over 200 people with advanced degrees in Statistics/Biostatistics.  Our diverse population of global talent brings innovation to every aspect of our business - from Discovery Research to Clinical Development to Manufacturing and Real-world Evidence.  We are playing a leading role in transforming the way the company develops medicines using state-of-the-art methods in adaptive designs, Bayesian statistics, causal inference, genetic/biomarker analysis, machine learning and more!  

The Clinical Project Statistician (Advisor - Statistics) develops or assists in the development of protocol designs, clinical plans, and data analysis plans in collaboration with physicians, clinical research scientists, and/or medical colleagues.  The Clinical Project Statistician is responsible for working with research associates and scientists to establish a reporting database, determining the appropriate statistical analysis procedures, and for analyzing data for clinical studies. 

Responsibilities:   

The job tasks listed below outline the scope of the position. The application of these tasks may vary, based upon current business needs. 

Statistical Trial Design and Analysis 

  • Operate in collaboration with study personnel to provide input on study protocol, design studies and write protocols for the conduct of each study.  

  • Assist in or be accountable for selecting statistical methods for data analysis, authoring the corresponding sections of the protocol and the statistical analysis plan, and conducting the actual analysis once a reporting database is created. 

  • Collaborate with data sciences in the planning and implementation of data quality assurance plans.  

  • Keep up to date with novel statistical methodology, maintain proficiency in applying new and varied methods, and to be competent in justifying methods selected. 

  • Influence team members regarding appropriate research methods 

  • Perform peer-review of work products from other statistical colleagues. 

  • Communication of Results and Inferences 

  • Collaborate with team members to write reports and communicate results.  

  • Assist with, or be responsible for, communicating study results via regulatory submissions, manuscripts, or oral presentations in group settings, as well as for communicating one-on-one with key customers and presenting at scientific meetings.  

  • Respond to regulatory queries and interact with regulators. 

  • Therapeutic Area Knowledge 

  • Understand disease states, competitive landscapes, and regulatory environment in order to enhance the level of customer focus and collaboration and be seen as a strong scientific contributor. 

  • Regulatory Compliance 

  • Perform work in full compliance with assigned curriculum(s) and will be responsible for following applicable Corporate, Medical, local, and departmental policies, procedures, processes, and training. 

  • Statistical leadership and Teamwork 

  • Introduce and apply innovative methodology and tools to solve critical problems 

  • Merge scientific thinking and business knowledge to identify issues, evaluate options and implement solutions. 

  • Lead projects independently and work effectively across functions.  Apply technical expertise to influence business decisions. 

Basic Qualifications  

  • Currently enrolled in and attending graduate school, and will complete a Ph.D. degree in Statistics OR Biostatistics  

  • Expected graduation by August 2026 

  • Must have successfully completed a previous internship with Lilly 

Additional Functional Job Skills & Preference  

  • Proficient in statistical programming languages/software such as SAS, R, Python, etc 

  • Interpersonal communication skills for effective customer consultation 

  • Teamwork and leadership skills 

  • Technical expertise and application with working knowledge of experimental design and statistical analysis 

  • Self-management skills with a focus on results for timely and accurate completion of competing deliverables 

  • Resource management skills  

  • Creativity and innovation  

  • Demonstrated problem solving ability and critical thinking 

  • Business process expertise associated with critical activities (e.g. regulatory submissions) 

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 Network, Black Employees at Lilly, Chinese Culture Network, Japanese International Leadership Network (JILN), Lilly India Network, Organization of Latinx at Lilly (OLA), PRIDE (LGBTQ+ Allies), Veterans Leadership Network (VLN), Women’s Initiative for Leading at Lilly (WILL), enAble (for people with disabilities). Learn more about all of our groups.

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

$151,500 - $222,200

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.

#WeAreLilly

Eli Lilly and Company

We're a medicine company turning science into healing to make life better for people around the world. It all started nearly 150 years ago with a clear vision from founder Colonel Eli Lilly: "Take what you find here and make it better and better." Harnessing the power of biotechnology, chemistry and genetic medicine, our scientists are urgently advancing science to solve some of the world's most significant health challenges. General Information and Guidelines: When you engage with us on LinkedIn, you're agreeing to these Community Guidelines: https://e.lilly/guidelines. If you have questions about a Lilly medicine, contact The Lilly Answers Center at 1-800-Lilly-Rx (1-800-545-5979) Monday through Friday, excluding company holidays.

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