Senior Statistician, Real-World Evidence (RWE)

BioSpace; Indianapolis (IN); On-site; USD 152,000 - 244,000; Full time

Job summary

Lilly, headquartered in Indianapolis, Indiana, seeks a Clinical Project Statistician to develop protocol designs and data analysis plans in collaboration with physicians and scientists. This role analyzes study data, writes analytical sections, and ensures regulatory readiness.

Responsibilities include leading statistical work, communicating results for submissions, and applying innovative methods. Strong RWE background and SAS/R proficiency are required.

Qualifications

• Ph.D. in Statistics, Biostatistics, Epidemiology, or Computer Science with 3+ years in Real World Evidence.
• Proficiency in SAS, R, Spotfire, WinBUGs and related tools.
• Strong interpersonal, teamwork and leadership abilities.

Responsibilities

• Design protocol, study design and analysis plans for clinical studies.
• Select statistical methods and write SAS/R sections of SAPs.
• Collaborate on data quality assurance and regulatory interactions.
• Lead projects and influence decisions across functions.

Skills

Statistical analysis

Data interpretation

Study design

Team leadership

Communication

Education

Ph.D. in Statistics/Biostatistics/Epidemiology/CS

Tools

SAS

R

Spotfire

WinBUGs

Job description

Lilly, headquartered in Indianapolis, Indiana, seeks a Clinical Project Statistician to develop protocol designs and data analysis plans in collaboration with physicians and scientists. This role analyzes study data, writes analytical sections, and ensures regulatory readiness.

Responsibilities include leading statistical work, communicating results for submissions, and applying innovative methods. Strong RWE background and SAS/R proficiency are required.