Director – AI Evidence Registry

100 Eli Lilly and Company; United States; Remote; USD 177,000 - 308,000; Full time

Benefits offered by this job

401(k)

Pension

Vacation benefits

Medical, dental, vision benefits

Flexible benefits

Life insurance

Job summary

Lilly seeks a Director, AI Evidence Registry to build and maintain a structured, AI-ready corpus of clinical evidence for Lilly medicines, designed for human readers and large language models. You will set the structure, standards, and quality controls powering the program.

You will collaborate with legal, regulatory, and business units to manage disclosure status, non-promotional standards, and ongoing registry updates as new evidence becomes available.

Qualifications

• Masters degree required in a relevant field.
• 8 years of experience in data science, statistical programming, biostatistics, or clinical informatics.
• 5 years in pharmaceutical/biotech/healthcare settings.

Responsibilities

• Develop and maintain a structured, AI-ready corpus of Lilly clinical evidence.
• Partner with business units to define standards and quality controls for registry scalability.
• Determine what evidence is eligible for external release with legal/regulatory review.
• Keep the registry current as new clinical evidence emerges.

Skills

Data standards experience

Linked data standards

Data specifications

Mentor technical staff

Education

Masters Degree in Data Sciences, Clinical Informatics, Computer Science, Biostatistics or Bioinformatics

Tools

CDISC SDTM/ADaM

JSON-LD/RDF/OWL/SHACL

Job description

At Lilly, the work is demanding because patients are waiting. We unite caring with discovery to help make life better for people around the world, knowing that every decision, every detail, and every day matters. Headquartered in Indianapolis, Indiana, our over 50,000 employees around the globe take on complex challenges to discover and deliver life-changing medicines, strengthen how health is understood and managed, and support the communities we serve. This is hard, urgent, selfless work—but it’s work worth doing. If you’re driven by purpose and ready to bring your best to work that truly matters for patients, we invite you to join us.

About

At Lilly, we believe in the extraordinary power of uniting care with discovery to make life better for people around the world. As a global healthcare leader headquartered in Indianapolis, we are driven by a deep sense of purpose—one that reaches far beyond our walls. Every day, our people bring passion, curiosity, and unwavering dedication to their work- discovering and delivering life-changing medicines, advancing the understanding of disease, and extending compassion into our communities through meaningful service and philanthropy. We're looking for individuals who share this purpose—who are inspired to make a lasting difference, and who are ready to help shape a better future for patients across the globe.

About Lilly Evidence Intelligence

Lilly Evidence Intelligence is a new function that delivers non-promotional and validated Lilly clinical evidence directly to the AI platforms healthcare providers increasingly rely on. The goal is to ensure that the responses healthcare providers receive reflect the most current, verified evidence available, at the speed clinical practice requires.

Position Overview

Lilly is seeking a Director, AI Evidence Registry that develops and maintains a structured, AI-ready body of clinical evidence on Lilly medicines, built for both human readers and large language models. This person defines the structure, standards, and quality of the evidence that powers the program.

How You Will Succeed

• Develop and maintain a structure, corpus of Lilly clinical evidence, optimized for accurate retrieval and interpretation by large language models.
• Partner with business units and relevant teams to define the standards and quality controls that govern the registry as it scales across the portfolio.
• Determine what evidence is eligible for external release, working with legal, and regulatory to confirm disclosure status and non-promotional standards before delivery.
• Keep the registry current as new clinical evidence emerges.

Basic Qualifications

• Masters Degree in Data Sciences, Clinical Informatics, Computer Science, Biostatistics or Bioinformatics
• 8 years of experience in data science, statistical programming, biostatistics, or clinical informatics
• 5 years in pharmaceutical, biotechnology, medical device, or healthcare provider settings.

Additional Skills/Preferences

• Experience authoring data specifications or interface specifications used by software engineering or data engineering teams.
• Experience producing analysis datasets, tables, figures, and listings from clinical trial data used in regulatory submissions or publications.
• Experience with CDISC data standards such as SDTM, ADaM, and CDISC controlled terminology.
• Experience with linked data or semantic web standards such as JSON-LD, RDF, OWL, or SHACL, including vocabulary and schema design.
• Has set technical standards or mentored other technical staff without formal reporting lines.

Disability Accommodation

Lilly is dedicated to helping individuals with disabilities to actively engage in the workforce, ensuring equal opportunities when vying for positions.

If you require accommodation to submit a resume for a position at Lilly, please complete the accommodation request form (https://careers.lilly.com/us/en/workplace-accommodation) for further assistance. Please note this is for individuals to request an accommodation as part of the application process and any other correspondence will not receive a response.

Equal Opportunity

Lilly is proud to be an EEO Employer and does not discriminate on the basis of age, race, color, religion, gender identity, sex, gender expression, sexual orientation, genetic information, ancestry, national origin, protected veteran status, disability, or any other legally protected status.

Employee Resource Groups (ERGs)

• Africa, Middle East, Central Asia (AMECA)
• Black Employees at Lilly (BE@Lilly)
• Chinese Culture Network (CCN)
• EnAble
• Evolve
• Lilly Indian Network (LIN)
• Organization of Latinx at Lilly (OLA)
• Pride (LGBTQ+ Allies)
• Veterans Leadership Network (VLN)
• Women’s Initiative for Leading at Lilly (WILL)

Compensation

Actual compensation will depend on a candidate’s education, experience, skills, and geographic location.

The anticipated wage for this position is $177,000 - $308,000.

Full-time equivalent employees also will be eligible for a company bonus (depending, in part, on company and individual performance).

Benefits

• company-sponsored 401(k)
• pension
• vacation benefits
• medical, dental, vision and prescription drug benefits
• flexible benefits (e.g., healthcare and/or dependent day care flexible spending accounts)
• life insurance and death benefits
• certain time off and leave of absence benefits
• well-being benefits (e.g., employee assistance program, fitness benefits, and employee clubs and activities)

Culture and Values

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! #WeAreLilly