Job Title: Senior / Advisor – Biostatistics
Category: Research & Development / Clinical Statistics
Location: Bangalore, Karnataka, India
Job Type: Full-Time, Regular
Experience Required: 3+ years in biostatistics/statistics with protocol design and clinical trial experience
Job ID: R-76298
About Lilly
At Eli Lilly and Company, we unite caring with discovery to improve lives worldwide. Headquartered in Indianapolis, Indiana, Lilly is a global healthcare leader committed to delivering life-changing medicines, advancing disease understanding, and fostering innovation in patient care. Our Bangalore capability center plays a key role in supporting global R&D and clinical development initiatives.
Role Overview
The Senior / Advisor – Biostatistics will serve as a strategic scientific partner in clinical trial design, data analysis, and statistical interpretation. You will work closely with physicians, medical colleagues, and research teams to ensure high-quality, compliant, and scientifically robust outcomes across Lilly’s clinical development portfolio.
This role requires hands-on experience in clinical trial statistics, protocol development, and data analysis, along with the ability to communicate results effectively to both internal stakeholders and external regulatory authorities.
Key Responsibilities
Statistical Trial Design & Analysis
Collaborate with study teams to design protocols, develop statistical methods, and plan analyses for clinical trials
Author statistical sections of clinical protocols and contribute to data analysis plans
Oversee data quality assurance in partnership with data management teams
Apply advanced statistical methods and maintain proficiency in new methodologies
Peer-review statistical outputs from colleagues to ensure accuracy and consistency
Results Communication & Reporting
Develop reports, manuscripts, and presentations to communicate study outcomes clearly and effectively
Present findings to internal teams, regulatory authorities, and at scientific meetings
Respond to regulatory queries and provide expert statistical input on study design and results
Therapeutic Area Expertise
Develop deep understanding of relevant disease states to enhance collaboration with clinical teams
Serve as a trusted scientific resource for stakeholders, providing insights that inform strategy and clinical decisions
Regulatory & Compliance Responsibilities
Ensure all work complies with global and local regulations, corporate policies, Good Clinical Practice (GCP), and departmental procedures
Qualifications
Minimum Requirements:
M.S. or Ph.D. in Statistics, Biostatistics, or equivalent
3+ years of relevant industry experience in clinical trial statistics, protocol design, or biostatistics
Proficiency in SAS programming and statistical software
Strong interpersonal and communication skills for stakeholder consultation
Ability to manage multiple priorities and deliver accurate, timely results
Preferred Skills & Attributes:
Experience in experimental design and advanced statistical methodologies
Leadership and mentoring experience within statistical or clinical teams
Strategic thinking, problem-solving, and business process expertise
Knowledge of regulatory submissions and clinical trial reporting standards
Why Join Lilly
Be part of a global leader in healthcare delivering life-changing medicines
Work in a dynamic R&D environment with international collaboration opportunities
Contribute to cutting-edge clinical research and therapeutic innovations
Thrive in a culture that emphasizes inclusion, professional development, and scientific excellence
Equal Opportunity Statement:
Lilly is committed to fostering an inclusive workforce. Individuals with disabilities are encouraged to apply and may request accommodations during the recruitment process via Lilly Accommodation Request.
Apply Now: Submit your CV and cover letter online via Lilly Careers Portal.
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Pondicherry (Puducherry) |Jharkhand :
Ranchi |Sikkim :
Rangpo |India :
Siliguri |Illinois :
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