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Senior Statistical Programmer

0-2 years
Not Disclosed
20 Nov. 17, 2025
Job Description
Job Type: Full Time Education: B.Sc/M.Sc/M.Pharma/B.Pharma/Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Senior Statistical Programmer

Location: Bangalore, Karnataka, India
Category: Research & Development
Job Type: Full Time – Regular
Job ID: R-95953


About Lilly

Lilly is a global healthcare leader headquartered in Indianapolis, Indiana. We work to discover and deliver life-changing medicines, advance disease understanding, and support communities through philanthropy and volunteerism.
We put people first and are committed to scientific excellence and innovation.


Role Overview

The Senior Statistical Programmer leads and supports programming activities for clinical trial data analysis, dataset creation (SDTM, ADaM), and production of statistical outputs (Tables, Listings, Graphs).
The role requires expertise in SAS programming, collaboration with cross-functional teams, and adherence to regulatory and quality standards.


Key Responsibilities

1. Statistical Trial Analysis

  • Lead all programming activities for clinical trial data analysis.

  • Create SDTM (Standard Data Tabulation Model) and ADaM (Analysis Data Model) datasets.

  • Generate statistical outputs: Tables, Listings, and Graphs (TLGs).

  • Support documentation tasks (e.g., Define.xml, Reviewer’s Guides, CRT packages).

  • Collaborate with statisticians and study teams to contribute to statistical analysis plans.

  • Assist in selecting appropriate statistical methods and authoring related documentation.

  • Perform analyses using the reporting database.

  • Work with Data Management on data quality assurance planning.

  • Stay updated on SAS programming techniques and statistical methodology.

  • Justify statistical methods and execute analysis plans accurately.

  • Peer-review the work of other programming/statistical colleagues.

  • Use current technologies and tools efficiently for trial analysis.


2. Communication of Results

  • Co-author and review study reports in collaboration with statistical colleagues.

  • Assist in communicating study results through:

    • Regulatory submissions

    • Manuscripts

    • Meetings and presentations

  • Respond to regulatory authority queries as needed.


3. Therapeutic Area & System Knowledge

  • Understand disease areas relevant to assigned studies to improve scientific quality and collaboration.

  • Ensure consistent and replicable use of tools, systems, and programming standards.

  • Stay updated on technological developments in statistical programming and clinical data systems.


4. Regulatory Compliance

  • Perform all work in full compliance with:

    • Assigned training curriculum

    • Corporate, medical, local, and departmental SOPs and guidelines

  • Follow all applicable policies, processes, and quality standards.


Diversity, Accessibility & Equal Opportunity

Lilly supports applicants with disabilities and provides reasonable accommodations during the application process.
The company does not discriminate based on age, race, gender, religion, sexual orientation, gender identity/expression, nationality, veteran status, disability, or any other legally protected category.