Principal Computational Statistician
Listed on 2026-08-23
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IT/Tech
Data Scientist, Data Analyst, Information Security & Data Protection
At Lilly, the work is demanding because patients are waiting. We unite caring with discovery to help make life better for people around the world, knowing that every decision, every detail, and every day matters. Headquartered in Indianapolis, Indiana, our over 50,000 employees around the globe take on complex challenges to discover and deliver life‑changing medicines, strengthen how health is understood and managed, and support the communities we serve.
This is hard, urgent, selfless work—but it’s work worth doing. If you’re driven by purpose and ready to bring your best to work that truly matters for patients, we invite you to join us.
At Lilly, we serve an extraordinary purpose. We make a difference for people around the globe by discovering, developing and delivering medicines that help them live longer, healthier, more active lives. Not only do we deliver breakthrough medications, but you also can count on us to develop creative solutions to support communities through philanthropy and volunteerism.
Responsibilities Statistical Analysis- Collaborate with other statistical colleagues and study personnel to provide input to statistical analysis plans, write reports and communicate results, assist/respond to regulatory queries.
- Assist in and/or be accountable for selecting statistical methods for data analysis, authoring the corresponding sections of the analysis plan, and conducting the actual analysis once a reporting database is created.
- Collaborate with data management in the planning and implementation of data quality assurance plans.
- Maintain proficiency with respect to SAS/R programming and statistical methodology and in applying new and varied methods.
- Effectively justify methods selected and implement previously outlined analysis plans.
- Conduct peer-review of work products from statistical colleagues.
- Effectively use current technologies and available tools for conducting the clinical trial analysis.
- Responsible for assisting in the communication of study results via regulatory submissions, and manuscripts, as well as for communicating one-on-one with key customers.
- Understand relevant disease states in order to enhance the level of customer focus and collaboration.
- Ensure replication of tools and systems, where applicable and stay informed of technological advances.
- Perform work in full compliance with assigned curriculum(s) and will be responsible for following applicable corporate, medical, local, and departmental policies, procedures, processes, and training.
- Master’s degree in Statistics, Biostatistics or MSPH with concentration in Statistics or Biostatistics, or relevant areas of science
- 2+ years of statistical analysis/programming experience
- Proficiency in statistical programming languages/software such as SAS, R, Spotfire, etc.
- Interpersonal/teamwork skills for effective interactions
- Technical growth and application with solid understanding of statistics and statistical software
- Self-management skills with a focus on results for prompt and accurate completion of competing deliverables
- Creativity and innovation
- Demonstrated problem solving ability and attention to detail.
- Data analysis, technology, and systems expertise
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