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Senior/ Advisor - Biostatistics

3+ years
Not Disclosed
10 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/Advisor – Biostatistics

Location: Bangalore, Karnataka, India
Category: Research & Development
Job Type: Full Time – Regular
Job ID: R-76298


About Lilly

At Lilly, we combine caring with scientific discovery to improve life for people worldwide. Headquartered in Indianapolis, Indiana, we develop and deliver life-changing medicines, advance disease understanding, and support communities through philanthropy and volunteer work.
We value people-first culture, scientific excellence, and impactful innovation.


Purpose of the Role

The Clinical Project Statistician collaborates with clinical teams to design study protocols, develop analysis plans, and analyze study data. The role includes working with scientists and research teams to build reporting databases and interpret study findings.


Key Responsibilities

1. Statistical Trial Design & Analysis

  • Collaborate with study teams to contribute to protocol design and study planning.

  • Design studies and write statistical sections of protocols.

  • Select appropriate statistical methods for data analysis.

  • Conduct statistical analyses using reporting databases.

  • Work with data management to implement data quality assurance plans.

  • Stay updated on statistical methodologies and justify method selections.

  • Peer-review work of other statisticians.

2. Communication of Results

  • Collaborate to write reports and interpret study outcomes.

  • Present study results in:

    • Regulatory submissions

    • Manuscripts

    • Scientific meetings & oral presentations

  • Respond to regulatory authority queries.

3. Therapeutic Area Knowledge

  • Understand relevant disease states to improve study relevance, contribute scientifically, and support cross-functional collaboration.

4. Regulatory Compliance

  • Ensure full compliance with all assigned training, corporate, medical, and departmental procedures.


Minimum Qualification Requirements

  • M.S. or Ph.D. in Statistics, Biostatistics, or equivalent.

  • More than 3 years of relevant experience.


Preferred Skills & Competencies

  • Proficiency in SAS programming.

  • Strong interpersonal and communication skills.

  • Effective teamwork and leadership qualities.

  • Knowledge of experimental design and advanced statistical methods.

  • Ability to manage multiple deliverables with accuracy and timeliness.

  • Strong problem-solving and strategic thinking.

  • Understanding of regulatory submission processes.

  • Creativity, innovation, and resource management abilities.


Additional Notes

Lilly provides equal employment opportunities and supports candidates with disabilities through accommodation requests during the application process.