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Lilly seeks a Technical Lead Architect to drive AI-enabled transformations across Global Regulatory Affairs and Global Scientific Communications. You will shape strategy, architecture, and security, while leading a team through complex pharma-regulatory projects.
This role combines hands-on execution with strategic leadership to modernize regulatory workflows, ensure compliance, and deliver scalable AI-enabled outcomes for patients globally.
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.
Technical Lead Architect - CTI MD Tech (GRA/GSC) Global Regulatory Affairs (GRA) · Global Scientific Communications (GSC) · CTI-MD Tech@Lilly Global Regulatory Affairs (GRA) and Global Scientific Communications (GSC) together own how Lilly's medicines move through health authority review, stay compliant once approved, and get communicated externally — spanning regulatory submissions, labelling, clinical trial disclosures, and scientific publications.
Both functions operate under strict compliance and audit-readiness requirements. The Technical Lead Architect (R5), GRA/GSC reimagines and transforms existing regulatory and scientific communications workflows into intelligent, agentic, AI-driven processes across the Global Regulatory Affairs (GRA) and Global Scientific Communications (GSC) portfolio. This role is split 70% hands‑on technical execution including coding and 30% strategy, and shapes the future technology landscape across regulatory, scientific communications, data, content, and digital capabilities — aligning business strategy with technology investment, AI innovation, and architecture to drive operational excellence, compliance, and scalable growth. This role ensures technology decisions across the portfolio align to a cohesive future‑state architecture, maximizing reuse, reducing complexity, and creating measurable business value.
Experience in both Global Regulatory Affairs and Scientific Communications. Familiarity with Regulatory Content and Submission Management, Veeva RIM, and regulatory platforms. Experience with document and content management ecosystems. Background in pharma and GxP-regulated environments.
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. 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! #WeAreLilly