Senior RWE Statistician – Clinical Trials Lead

100 Eli Lilly and Company; Indianapolis (IN); On-site; USD 152,000 - 244,000; Full time

Benefits offered by this job

401(k)

Pension

Vacation

Health benefits

Flexible benefits

Life insurance

Time off

Well-being programs

Job summary

Eli Lilly and Company is seeking a Clinical Project Statistician to design studies, analyze data, and report results in collaboration with physicians and research teams. You will lead methodological choices, ensure data quality, and communicate findings for regulatory submissions and scientific meetings.

Responsibilities include protocol input, statistical analysis planning, and cross-functional coordination to advance clinical studies while maintaining regulatory compliance and scientific rigor.

Qualifications

• Ph.D. in Statistics/Biostatistics/Epidemiology/CS with 3+ years in Real World Evidence research.
• Proficient in SAS, R, Spotfire, WinBUGs or similar.
• Strong communication for customer consultation.
• Teamwork and leadership skills.
• Working knowledge of experimental design and statistical analysis.
• Self-management with timely delivery of deliverables.
• Resource management skills.
• Creativity and innovation.
• Demonstrated problem solving and critical thinking.

Responsibilities

• Design studies and write protocols for conduct of each study; select statistical methods.
• Collaborate with data sciences on data quality assurance and methodology.
• Communicate results via regulatory submissions, manuscripts, or presentations.
• Understand disease areas, regulatory environments to inform analysis.
• Ensure compliance with corporate and departmental policies.

Skills

Interpersonal skills

Team leadership

Statistical methods

Self-management

Resource management

Creativity

Problem solving

Education

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

Tools

SAS

R

Spotfire

WinBUGs

Job description

Eli Lilly and Company is seeking a Clinical Project Statistician to design studies, analyze data, and report results in collaboration with physicians and research teams. You will lead methodological choices, ensure data quality, and communicate findings for regulatory submissions and scientific meetings.

Responsibilities include protocol input, statistical analysis planning, and cross-functional coordination to advance clinical studies while maintaining regulatory compliance and scientific rigor.