Sr. Advisor - Statistics

Eli Lilly Eli Lilly · Pharma · Indianapolis, IN

This role focuses on statistical trial design and analysis within clinical research and development in the healthcare domain. The primary responsibilities include developing protocol designs, writing protocols, selecting statistical methods, analyzing clinical study data, and communicating results. The role requires a Ph.D. in Statistics or Biostatistics with experience in clinical R&D and proficiency in statistical programming languages.

What you'd actually do

  1. Provide input on study protocol, design studies and write protocols for the conduct of each study.
  2. Be accountable for selecting statistical methods for data analysis, authoring the corresponding sections of the protocol and the statistical analysis plan, and conducting the actual analysis once a reporting database is created.
  3. Collaborate with data sciences in the planning and implementation of data quality assurance plans.
  4. Maintain currency with respect to statistical methodology, maintain proficiency in applying new and varied methods, and to be competent in justifying methods selected.
  5. Perform peer-review of work products from other statistical colleagues.

Skills

Required

  • Ph.D. in Statistics or Biostatistics
  • 3 years of experience in Clinical Research and Development
  • Statistical Trial Design
  • Data Analysis
  • SAS
  • R

Nice to have

  • Spotfire
  • WinBUGs
  • Interpersonal communication skills
  • Teamwork and leadership skills
  • Technical expertise and application with working knowledge of experimental design and statistical analysis
  • Self-management skills
  • Resource management skills
  • Creativity and innovation
  • Demonstrated problem solving ability and critical thinking

What the JD emphasized

  • Ph.D. in Statistics OR Biostatistics with at least 3 years of experience in Clinical Research and Development