• Document, maintain, and govern end-to-end business processes and data flows using standardized modeling tools, ensuring consistency, traceability, and readiness for analysis or optimization. • Translate current-state and future-state processes into clear visual models that support operational excellence, regulatory compliance, and business decision-making. • Partner with cross-functional stakeholders to design, optimize, and improve processes, systems, training, and communications aligned to strategic initiatives. • Lead small to medium-scale process improvement initiatives, from problem definition through solution design and implementation. • Analyze process performance, identify gaps or risks, and prioritize improvement opportunities based on business impact and compliance needs. • Review and guide updates to procedural documentation to ensure alignment with defined processes and regulatory expectations. • Develop supporting materials, presentations, and tools to enable adoption and sustainability of optimized processes. • Provide guidance and mentoring to junior team members, promoting consistent process standards and best practices.

• Proactively collaborate with initiative leads and management to prepare, organize, coordinate, document and/or provide the development and delivery of department products and services to a globally dispersed, cross-functional audience in support of business outcomes and industry compliance requirements. • Develop varied support materials, presentations, and/or tools to support department's remit and strategies. • Proactively collaborate with initiative leads and management to develop, optimize and improve processes, associated systems/applications, training and communications. • Lead small to medium-scale process improvement initiatives. • Develop process improvement processes and solutions. • Identify and collate information required to assess compliance with processes and to prioritize business process improvement needs. • May review, assess and update procedural documents for overall compliance with current processes. • Perform special projects, assignments and administrative tasks per business needs.

• The Clinical Research Lead (CRL) is a strategic, field-based scientific leader responsible for driving the execution of Lilly clinical trials through exceptional investigator engagement and site performance management • Accountable for the full spectrum of investigator engagement from identification and qualification through enrollment, and support database lock, and study closeout • Serve as a clinical trial scientific ambassador, ensuring investigators deeply understand protocol intent, scientific rationale, and patient eligibility requirements • Develop and sustain strategic, high-trust relationships with investigators that span trials and therapeutic areas • Influence enrollment by co-creating tailored recruitment strategies aligned with site capabilities, patient population realities, and study objectives • Proactively find opportunities to reach new patients, accelerate enrollment and increase impact at priority sites, including for example, novel site models, community-based research initiatives etc • Capture and elevate critical insights from sites to optimize feasibility, protocol design, and study conduct • Lead site-level strategy and risk planning to ensure strong and predictable enrollment and data delivery • Leverage performance metrics to anticipate issues, intervene decisively, and maintain momentum toward clinical milestones • Drive inspection readiness as a continuous discipline across sites • Collaborate across functions and with vendor partners to resolve operational barriers, ensuring delivery with speed and quality • Provide oversight and quality assurance for vendor monitoring, escalating risks proactively • Act as a key liaison between field teams, vendors, and investigators, ensuring alignment, shared purpose, and continuous knowledge transfer

• Designing and implementing clinical trial protocols, ensuring adherence to scientific and regulatory standards. • Conducting data analysis and interpretation to derive insights that support study objectives. • Collaborating with cross-functional teams to ensure effective study execution and data quality. • Engaging with stakeholders to communicate findings and contribute to scientific discussions. • Assisting in the preparation of regulatory submissions, study reports, and scientific publications.