Sr. Director- Trial Management

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.  Verve Therapeutics, a Lilly Research Labs subsidiary, is a clinical-stage genetic medicines company on a mission to solve cardiovascular disease. Founded by leaders in cardiovascular medicine and gene editing, Verve is developing one-time gene editing treatments aimed at turning chronic management into a single-course cure. Its lead programs target PCSK9 and ANGPTL3 to lower LDL-C, the root cause of cardiovascular disease. The Senior Director, Trial Management provides strategic and operational leadership for the trial management function across Verve’s early development gene editing clinical programs. This role leads trial management leaders, strengthens consistency in execution, and advances standard practices to support high-quality, efficient, and compliant delivery. This leader will play a key role in harmonizing ways of working across Verve and Lilly processes, helping build an integrated operating model that enables clarity, speed, and quality across the portfolio. As a member of the Development Operations leadership team, this individual will contribute to broader functional priorities, organizational decisions, and cross-functional alignment.

Lead and develop trial management leaders, setting clear expectations for performance, collaboration, and execution Standardize and continuously improve trial management best practices, tools, and operating rhythms across programs Drive harmonization of trial management processes across Verve and Lilly to support a consistent and scalable operating model Serve as an active member of the Clinical Development Operations leadership team, contributing to strategic planning, organizational effectiveness, and functional direction Provide oversight across clinical programs to ensure delivery against timelines, quality expectations, budgets, and study goals Partner closely with cross-functional team members including Clinical Development, Regulatory, Data Management, Patient recruitment /retention, Study start up, Medical Writing, Supply Chain, Quality, Clinical Compliance, and other key functions to support aligned study execution Work with Compliance and Oversight to strengthen governance, escalation, and decision-making processes to identify and address operational risks early Ensure teams apply a risk-based approach to planning, study oversight, and issue resolution Oversee CRO and vendor strategy within the function, including expectations for performance, partnership, and accountability Support development and refinement of SOPs, workflows, and business processes that promote quality, compliance, and consistency across trials and programs Champion compliance with GCP, ICH, and applicable global regulatory requirements, while supporting inspection readiness Monitor key operational metrics and use data-driven insights to improve execution, resource planning, and leadership visibility Foster a culture aligned with Team Lilly expectations, including collaboration, accountability, inclusion, and continuous improvement Coach, mentor, and develop talent within the trial management organization to strengthen capability and succession depth Represent the trial management function in cross-functional and leadership forums Basic Qualifications Bachelor’s degree in a scientific, healthcare, or related discipline required;