Senior/Principal Statistical Programmer
Eli Lilly and Company (company site, opens in a new tab)BengaluruOn-siteDirect career pageEst. 22–40 LPA
Posted 19h ago
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Job description
Structured overview of role & requirements
About This Role
- Conduct sample size calculations and quantitative assessments to support clinical study designs.
- Develop CDISC-compliant (ADaM/SDTM) submission-ready datasets and execute statistical analysis plans to support clinical development and regulatory submissions.
- Produce formal technical reports and presentations summarizing analyses for technical leaders and management, while ensuring regulatory compliance and data integrity.
Minimum Requirements
- Experience Required: Not explicitly mentioned in the JD.
- Proficiency in statistical analysis and programming relevant to clinical data (including CDISC standards).
- Ability to develop and validate statistical programming code and outputs for clinical submissions.
- Location and notice period requirements: Not explicitly mentioned in the JD.
Ideal Candidate Profile
- Experienced in applying defined statistical methods to routine clinical data analyses and study design support.
- Skilled in cross-functional collaboration to influence technical decisions and promote data-driven analytics.
- Familiarity with regulatory requirements, data integrity and validation concepts in clinical research and computerized systems.