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Lilly Statistical Programmer / Senior Statistical Programmer in Bengaluru, India

At Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our 35,000 employees around the world work to discover and bring life-changing medicines to those who need them, improve the understanding and management of disease, and give back to our communities through philanthropy and volunteerism. We give our best effort to our work, and we put people first. We’re looking for people who are determined to make life better for people around the world.

The job tasks listed below outline the scope of the position. The application of these tasks may vary, based on current business needs.

Statistical Trial Analysis

Support all programming activities required for the data analysis of the clinical trials and create standard datasets (SDTM) and analysis datasets (ADaM) and generate reports of the form Tables, Listings and Graphs are applicable.

Support other documentation tasks such as Define, RGs and CRT packages as required for the reporting of clinical trials.

Collaborate with other statistical colleagues and study personnel to provide input to statistical analysis plans.

Assist in and/or be accountable for selecting statistical methods for data analysis, authoring the corresponding sections of the data analysis plan, and conducting the actual analysis once a reporting database is created.

Collaborate with data management in the planning and implementation of data quality assurance plans.

Maintain proficiency with respect to SAS programming and statistical methodology and in applying new and varied methods.

Effectively justify methods selected and implement previously outlined analysis plans.

Conduct peer-review of work products from statistical colleagues.

Effectively utilize current technologies and available tools for conducting the clinical trial analysis. Communication of Results and Inferences

Collaborate with other statistical colleagues to write reports and communicate results.

Responsible for assisting in the communication of study results via regulatory submissions, and manuscripts, as well as for communicating one-on-one with key customers.

Assist or respond to regulatory queries working in collaboration with other statistical colleagues. Therapeutic Area and Systems Knowledge

Understand relevant disease states in order to enhance the level of customer focus and collaboration.

Ensure replication of tools and systems, where applicable and stay informed of technology advances.

Regulatory Compliance

Perform work in full compliance with assigned curriculum(s) and will be responsible for following applicable Corporate, Medical, local, and departmental policies, procedures, processes and training.

Eli Lilly and Company, Lilly USA, LLC and our wholly owned subsidiaries (collectively “Lilly”) are committed to help individuals with disabilities to participate in the workforce and ensure equal opportunity to compete for jobs. If you require an accommodation to submit a resume for positions at Lilly, please email Lilly Human Resources ( ) for further assistance. Please note This email address is intended for use only to request an accommodation as part of the application process. Any other correspondence will not receive a response.

Lilly does not discriminate on the basis of age, race, color, religion, gender, sexual orientation, gender identity, gender expression, national origin, protected veteran status, disability or any other legally protected status.


At Lilly we strive to ensure our employees are part of a team that cares about them and our shared purpose of making life better for those around the world. How do we do this? We continue to look for ways to include, innovate, accelerate and deliver while maintaining integrity, excellence and respect for people.​ We hope that you seek to join us on our journey as we create medicine and deliver improved outcomes for patients across the globe!