Global Regulatory Lead, Regulatory Strategy - Global Regulatory Affairs - Infectious Disease/Vaccine

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.

As the Global Regulatory Lead (GRL), you will be the accountable decision maker for the development & execution of global regulatory strategies— from portfolio entry through end of life. You will provide strategic and technical leadership to a cross-functional Global Regulatory Team , serve as the primary regulatory voice on the Global Brand Development (GBD) team, and own the relationship and interaction strategy with the US FDA.

Regulatory Strategy Develop and execute innovative global regulatory strategies, owning the Regulatory Strategy Document (RSD) from Candidate Selection through end of lifecycle Integrate competitive intelligence, health authority guidance, and product-specific regulatory advice to drive robust, forward-looking strategies Lead regulatory representation on the GBD/global program team, shaping development plans and providing solutions to regulatory barriers Ensure local affiliate regulatory plans align to global strategy and business priorities — spanning labeling, risk management, and issues management US FDA Oversight Oversee all US FDA submissions and agency interactions, including INDs, NDAs, and BLAs Drive high-quality communications with FDA that clearly articulate Lilly's scientific position Build and leverage productive relationships with FDA to support product registration goals Cross-Functional Team Leadership Provide strategic direction to a cross-functional Global Regulatory Team inclusive of regional scientists, GRA-CMC, GRA-Devices, GRA-RD&E, and Global Labeling Foster a culture of transparent communication, feedback, and continuous development Communicate and share key information to enable seamless execution of global regulatory strategy and cross-functional shared learnings. Represent GRA at stakeholder and governance meetings; mentor GRA personnel External Engagement Shape the external regulatory environment by building strategic relationships with key external stakeholders Partner with Regulatory Product Communications and Global Marketing to advise on promotional strategy and review press/IR materials Minimum Qualifications Advanced scientific degree (i.e. PharmD, PhD) and 8+ years of experience in regulatory affairs and/or drug development OR Bachelor’s or Masters and 10+ years of experience in regulatory affairs and/or drug development Additional Preferences Deep knowledge of global regulatory procedures, evolving reform initiatives, and the integrated drug development process Demonstrated experience with regulatory submissions and agency interactions across US, EU, China, and Japan Direct experience in both clinical and CMC regulatory sciences Strong leadership, negotiation, and stakeholder communication skills — including executive-level audiences Proven ability to assess and manage risk in a highly regulated environment Experience in the applicable therapeutic area Additional Information Travel expected: 10–15% 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