Instagram
youtube
Facebook

Biostatistician (R6-R7)

5+ years
$84,240 annually.
10 April 28, 2025
Job Description
Job Type: Full Time Education: Master’s degree Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

 

Job Title

Biostatistician (R6-R7)

Location

Indianapolis, Indiana, United States

Company

Eli Lilly and Company

Category

Research & Development

Job Type

Full Time | Regular

Job ID

R-83574

Position Summary

The Biostatistician (R6-R7) will serve as a study statistician within the clinical and development teams. The role involves performing ad hoc analyses, supporting the statistical programming team, ensuring proper statistical methodology implementation, and designing data capture methods for clinical programs. The individual will also contribute to the development of policies, procedures, and standards within the biostatistics department.

Key Responsibilities

Statistical Analysis and Programming:

  • Perform ad hoc analyses and ensure the appropriate use of statistical methodologies.

  • Develop statistical programs for analysis, data displays, and verification of data and analyses.

Clinical Trial Design:

  • Design data capture methods and select appropriate study endpoints for clinical programs.

  • Contribute to clinical trial design and regulatory processes related to statistical analysis.

Team Collaboration:

  • Work collaboratively with cross-functional clinical and development teams.

Policy Development:

  • Contribute to the development of policies, procedures, and standards within the biostatistics department.

Education and Experience

  • Master’s degree in Statistics, Biostatistics, or a related field.

  • 5 years of experience in biostatistics for clinical development in the pharmaceutical or biotech industry.

  • Minimum of 3 years of experience in clinical trial design, drug development regulations, SAS programming, and statistical analysis for oncology research.

Additional Skills/Preferences

  • 3 years of experience with clinical trial design and statistical analysis for oncology research.

  • Proficiency in SAS programming and CDISC models and standards.

  • Strong knowledge of statistical applications in clinical trials.

Compensation

  • Anticipated Salary: $84,240 annually.

  • Eligible for company bonus program (based on company and individual performance).

Benefits

  • 401(k) plan and pension

  • Vacation and paid time off

  • Medical, dental, vision, and prescription drug benefits

  • Flexible spending accounts (healthcare, dependent care)

  • Life insurance and death benefits

  • Wellness programs (EAP, fitness benefits, clubs, and activities)

  • Other leave of absence benefits

Travel

  • 5% domestic travel required.

Telecommuting

  • Telecommuting benefit available.

On-Site Position

  • Located at Indianapolis, IN.

Equal Opportunity Employer

Lilly is an equal opportunity employer dedicated to diversity and inclusion.

Employee Resource Groups (ERGs)

Includes groups such as Black Employees at Lilly, Organization of Latinx at Lilly (OLA), Lilly India Network, PRIDE (LGBTQ+ Allies), Women’s Initiative for Leading at Lilly (WILL), and others.

Accommodation

Applicants needing accommodations during the application process can request assistance via the Accommodation Request Form.