Senior/Principal Statistical Programmer
Eli Lilly and CompanyMatch Score
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Job Description
Structured overview of role & requirementsAbout This Role
Lead and execute programming for clinical trial data analysis including creation of SDTM and ADaM datasets and generation of tables, listings, and graphs.
Contribute to statistical analysis planning, selection and justification of methods, and conduct analysis aligned with reporting databases.
Collaborate with stakeholders to communicate study results through regulatory submissions, reports, and handle related queries.
Minimum Requirements
Proficient in SAS programming and statistical methods applied to clinical trial data.
Experience with standard clinical trial data standards such as SDTM and ADaM for dataset creation and reporting.
Knowledge of regulatory documentation related to clinical trials including Define.xml, RGs, and CRT packages.
Work Experience Required: Not explicitly mentioned in the JD.
Ideal Candidate Profile
Strong expertise in statistical programming and analysis within a clinical research environment supporting regulatory submissions.
Ability to navigate complex interdisciplinary collaboration with statisticians, data management, and clinical study teams.
Experienced in applying and explaining statistical methodology and quality assurance in clinical trial programming and reporting.