Senior RWE Statistician — Clinical Trials & Analytics

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

Benefits offered by this job

401(k) plan

Pension

Vacation benefits

Medical, dental, vision benefits

Flexible benefits

Life insurance

Well-being programs

Job summary

Lilly in Indianapolis, Indiana, seeks a Clinical Project Statistician to lead statistical design and analysis for clinical trials. You will work with physicians and researchers to craft protocols, analysis plans, and reporting databases, ensuring data quality and regulatory readiness.

The role requires a PhD with Real World Evidence experience and strong collaboration skills. You will communicate results through reports, manuscripts, and presentations, and contribute to regulatory questions and

Qualifications

• PhD in Statistics/Biostatistics, Epidemiology or CS with 3+ years Real World Evidence experience.
• Proficient in SAS, R, Spotfire, WinBUGs for analyses.
• Strong communication, teamwork and problem solving abilities.

Responsibilities

• Design study protocols and statistical plans for clinical trials.
• Analyze data and report results for regulatory submissions and publications.
• Collaborate across functions to implement data quality assurance.
• Lead projects and influence decisions with statistical expertise.
• Maintain up-to-date knowledge of statistical methods and regulatory expectations.

Skills

Statistical programming

Interpersonal communication

Teamwork & leadership

Experimental design & statistics

Self-management & reliability

Problem solving & critical thinking

Creativity & innovation

Resource management

Education

PhD in Statistics/Biostatistics/Epidemiology/CS

Tools

SAS

R

Spotfire

WinBUGs

Job description

Lilly in Indianapolis, Indiana, seeks a Clinical Project Statistician to lead statistical design and analysis for clinical trials. You will work with physicians and researchers to craft protocols, analysis plans, and reporting databases, ensuring data quality and regulatory readiness.

The role requires a PhD with Real World Evidence experience and strong collaboration skills. You will communicate results through reports, manuscripts, and presentations, and contribute to regulatory questions and