• Partner with Medical Affairs leadership to establish priorities, operational plans, and strategic investments. • Develop business reviews, leadership presentations, dashboards, operational metrics, and reporting. • Develop and continuously improve processes, governance, operating models, and performance metrics. • Identify operational risks, dependencies, and resource needs. • Oversee Medical Affairs operational support and vendor management. • Serve as the primary operational liaison between Medical Affairs and key cross-functional partners. • Lead and coordinate cross-functional initiatives that advance Medical Affairs strategy. • Build strong relationships across a complex matrixed organization.

• Lead execution of pivotal clinical trials • Serve as Study Responsible Physician and provide medical oversight for one or more Phase 3 clinical studies supporting the late-stage development of ELVN-001. • Provide leadership, mentoring, and oversight to clinical scientists across assigned studies and development activities. • Partner cross-functionally with Clinical Operations, Biostatistics, Clinical Pharmacology, Regulatory Affairs, Translational Sciences, Data Management, and other functions to ensure high-quality and timely study execution. • Contribute to the design, conduct, analysis, and interpretation of late-stage oncology clinical trials. • Lead ongoing medical monitoring activities, including safety review, data interpretation, benefit-risk evaluation, protocol deviation review, and endpoint adjudication. • Collaborate with clinical scientists and cross-functional partners on: Preparation and review of clinical study documents, including protocols, amendments, investigator brochures, informed consent forms, and clinical study reports. Medical review of clinical data and support of data review activities. Preparation and presentation of clinical data for internal governance meetings, investigator meetings, scientific congresses, and external stakeholder interactions. Development of study-related training materials and investigator communications. Support regulatory submissions and responses to Health Authority and Ethics Committee inquiries. Build and maintain relationships with clinical investigators, cooperative groups, and Key Opinion Leaders. Contribute to registrational clinical development strategy, Phase 3 execution, commercialization planning and lifecycle planning for oncology programs. Participate in preparation of scientific publications, abstracts, and presentations. Review and synthesize relevant scientific and medical literature to support program strategy and competitive awareness. Support broader clinical development and medical affairs initiatives as needed.

• The Associate Director Clinical Scientist contributes to the execution of the clinical development plan for candidate drug products in collaboration with Project Leaders and Medical Directors. • The clinical scientist will be involved in operationalizing studies, monitoring data in real time to ensure the integrity of the study and proactively identifying issues in the conduct of trials. • Responsible for medical review and data analysis for the purposes of both data cleaning and interpretation for regulatory documents and publications. • Monitoring of clinical data: Perform high level clinical data review for quality and patient safety on an ongoing basis and escalate issues to the medical director as appropriate. • Work collaboratively with data management, clinical operations, and medical monitors to ensure clinical data review is performed efficiently and in alignment with the needs of the trial. • Generate and review clinical documents including concept sheets/decks, clinical study protocols, investigator brochures, and regulatory documents. • Organize and present data, study designs, and other information to advisory boards, investigator meetings, site interactions, study committees, and other internal and external settings.

• Recruit, develop, and lead a high-performing Endoluminal Clinical Sales team across the Europe Direct Region. • Drive execution of the Ion commercial strategy to achieve and exceed procedural growth, revenue, and organizational goals. • Coach and support Endoluminal Program Managers (EPMs) in performance management of QBR/ETA teams. • Foster a culture of accountability, collaboration, innovation, and continuous improvement aligned with Intuitive's mission and values. • Drive strong cross-functional collaboration and alignment across teams. • Maintain team focus and commitment to the defined Ion commercial strategy. • Partner closely with Endoluminal Sales Directors (ESDs) and Endoluminal Sales Managers (ESMs) to deliver best-in-class customer experience and maximize customer success. • Develop and maintain strategic relationships with physician leaders, executive stakeholders, and key opinion leaders to accelerate market adoption and advocacy. • Identify, scale, and implement best practices, programs, and processes that support accelerated growth of the Ion procedure business. • Effectively allocate and leverage organizational resources to achieve commercial objectives while maintaining budget discipline. • Drive a solution-focused culture in a dynamic and challenging environment.