• 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.

• The Senior Director, Vaccines Retail Channel Medical Lead is a senior, field‑based medical leader within the Vaccines Field Medical organization, responsible for enterprise‑level medical engagement across the U.S. retail pharmacy and retail healthcare channel. • Support the development and delivery of objective, scientifically sound medical information tailored to national retail partners, addressing Pfizer’s vaccines and the diseases they prevent. • Collaborating closely with cross-function medical partners to identify vaccine specific medical education and project needs. • Compliantly execute mutually beneficial, retail stakeholder‑specific medical projects, collaborations, strategic medical partnerships, and non‑interventional studies that align with vaccine‑specific business and public health needs. • Build and sustain strategic, longitudinal medical partnerships with national and regional retail pharmacy chains and retail healthcare organizations that influence vaccination delivery models, access strategies, and population‑level immunization outcomes.

• Define and execute the clinical platforms product strategy and roadmap, aligned to Fortrea’s enterprise and clinical delivery objectives. • Lead end-to-end product development lifecycle, including ideation, engineering, validation, deployment, and lifecycle management of applications. • Drive adoption of a product-centric operating model (agile, DevOps, customer-first delivery). • Ensure solutions are scalable, secure, and compliant with regulatory requirements within clinical research. • Evaluate and integrate digital health, AI/ML, and emerging technologies to enhance clinical trial and delivery and patient experience. • Continuously evaluate market trends, competitive landscape, and technology trends to ensure Fortrea maintains competitive position in the marker. • Lead the day-to-day operating model for Clinical Platforms, ensuring delivery predictability, quality, and efficiency. • Own PMO governance, portfolio prioritization, and execution discipline across platform initiatives. • Establish consistent delivery standards, reporting cadence, and performance metrics. • Proactively identify and mitigate risks, dependencies, and resource constraints. • Ensure alignment between product roadmaps and delivery capacity. • Drive continuous improvement in delivery speed, cost efficiency, and quality outcomes. • Ensure platforms support the end-to-end clinical trial lifecycle, including study startup, site management, data capture, monitoring, safety, and regulatory submission. • Translate clinical and operational needs into technology-enabled solutions that improve efficiency, compliance, and data integrity. • Act as the primary integrator across Clinical Operations, Commercial, Quality, Regulatory, Security, and Data Privacy. • Partner with business leaders to ensure clear accountability, governance, and decision-making across complex initiatives. • Own development of executive-level communications, presentations, and external-facing materials. • Build and maintain a standardized library of platform assets (decks, demos, one-pagers).