Lead Clinical Project Statistician

Eli Lilly and Company; Indianapolis (IN); On-site; USD 153,000 - 246,000; Full time

Benefits offered by this job

401(k) plan

Pension

Medical, dental, vision benefits

Life insurance

Well-being programs

Job summary

Lilly is seeking a Clinical Project Statistician to develop protocol designs, analytics plans, and to analyze data for clinical studies. The role involves collaborating across teams to ensure data quality, communicating results for regulatory submissions, and applying innovative statistical methods to solve complex problems.

The position requires a Ph.D. in Statistics or Biostatistics with at least 3 years in Clinical Research and Development, and proficiency in SAS, R, Spotfire, and WinBUGs.

Qualifications

• Ph.D. in Statistics OR Biostatistics with at least 3 years in Clinical Research and Development.
• Proficient in SAS, R, Spotfire, WinBUGs.
• Strong interpersonal communication and teamwork skills.
• Leadership skills with ability to influence.
• Technical expertise in experimental design and statistical analysis.
• Self-management and ability to deliver multiple deliverables on time.
• Resource management and problem solving abilities.
• Creativity and innovation in applying methodology.
• Demonstrated critical thinking and problem solving abilities.

Responsibilities

• Design studies and write protocols and statistical analysis plans.
• Perform data analyses and interpret results for reporting and regulatory submissions.
• Collaborate with data sciences to ensure data quality and analysis integrity.
• Communicate results via reports, manuscripts, and presentations.
• Ensure compliance with regulatory and internal policies.

Skills

Interpersonal communication

Teamwork and leadership

Creativity and innovation

Problem solving

Self-management

Resource management

Critical thinking

Education

Ph.D. in Statistics or Biostatistics

Tools

SAS

R

Spotfire

WinBUGs

Job description

Lilly is seeking a Clinical Project Statistician to develop protocol designs, analytics plans, and to analyze data for clinical studies. The role involves collaborating across teams to ensure data quality, communicating results for regulatory submissions, and applying innovative statistical methods to solve complex problems.

The position requires a Ph.D. in Statistics or Biostatistics with at least 3 years in Clinical Research and Development, and proficiency in SAS, R, Spotfire, and WinBUGs.