Clinical Trial Statistics Advisor

JobsInSAS.com; Indianapolis (IN); On-site; USD 152,000 - 244,000; Full time

Benefits offered by this job

Company bonus

401(k) plan

Medical, dental, vision benefits

Job summary

Lilly in Indianapolis, Indiana, seeks an Advisor - Statistics to lead protocol design, data analysis plans, and database reporting for clinical studies. You will drive statistical trial design, execute analyses, and communicate results to teams and regulators.

The role requires a Ph.D. in Statistics or Biostatistics and experience in Clinical Research and Development, with proficiency in SAS/R/Spotfire/WinBUGs and strong collaboration and leadership skills.

Qualifications

• PhD in Statistics or Biostatistics with at least 2 years of clinical R&D experience.
• Proficient in SAS, R, Spotfire, WinBUGs or similar statistical tools.
• Strong communication and collaboration skills.
• Ability to lead projects and apply innovative methods.

Responsibilities

• Design study protocols and analysis plans for clinical trials.
• Select statistical methods and conduct analyses for reporting databases.
• Collaborate with data sciences on data quality assurance.
• Present results for regulatory submissions and scientific meetings.

Skills

Interpersonal comms

Team leadership

Creativity

Problem solving

Self-management

Resource mgmt

Education

Ph.D. in Statistics or Biostatistics

Tools

SAS

R

Spotfire

WinBUGs

Job description

Lilly in Indianapolis, Indiana, seeks an Advisor - Statistics to lead protocol design, data analysis plans, and database reporting for clinical studies. You will drive statistical trial design, execute analyses, and communicate results to teams and regulators.

The role requires a Ph.D. in Statistics or Biostatistics and experience in Clinical Research and Development, with proficiency in SAS/R/Spotfire/WinBUGs and strong collaboration and leadership skills.