• This strategic leader is responsible for architecting safe, reliable, and human-centered clinical workflows across the enterprise. • This role focuses on designing and standardizing high-risk clinical processes, integrating human factors, and embedding reliability principles to ensure that healthcare teams can consistently deliver safe, efficient, and high-quality care. • The Director serves as a systems design authority, partnering with clinical leaders, operations, IT, supply chain, and other key stakeholders to proactively reduce risk and optimize clinical care. • Lead system-level clinical workflow design and standardization for high-risk processes. • Collaborate with Continuous improvement and Safety teams to translate lessons from events and performance data into systemic design improvements. • Define and monitor reliability thresholds for critical clinical processes. • Partner with key stakeholders including IT, facilities, operations, and clinical leaders to review and approve major workflow and technology projects from a safety and reliability perspective. • Ensure clinical design solutions are scalable, sustainable, and aligned with enterprise safety, reliability, and performance goals. • Integrate human factors and human-centered design principles into all clinical system changes. • Provide thought leadership and education in clinical systems design, human factors, and safety engineering within the organization.

• Supporting Pfizer Oncology as the Director of Site Management and Monitoring • Ensure appropriate Site Care Partner (SCP) resources are in place for country and site-level study startup and management • Collaborate with cross-functional teams for country and site selection, regulatory approvals, and study management • Drive effective resource management across portfolio for balanced SCP and site monitors allocation • Demonstrate leadership in resolving site/country/cluster/regional issues to maintain site start-up and quality • Establish consistent direction and priorities across assigned countries/cluster/region • Responsible for timely and quality site activation and monitoring activities • Mitigate systematic deficiencies in clinical trial conduct to improve quality and patient safety

• Provide the day-to-day leadership and management of Account Management Colleagues • Co-lead brand IPT working with account marketing team to support KAM strategy, goals, and KPIs. • Take full accountability for all personnel issues and act as the final point of escalation for all Account Management roles in their region • Lead the consistent execution business and account priorities within the region • Deliver documented capabilities-based coaching to support skill excellence and optimal development across the KAM team. • Manage the various budgets for the assigned region. • Maintain required technical, environmental and Account Management expertise to respond accurately and compliantly to all questions • Recruit and select candidates for Account Management positions in compliance with Pfizer requirements

• Responsible to plan, manage, organize, evaluate and/or report on the day delivery of the Clinical Monitoring unit (Clinical Operations Leads). • Role includes policy and process development and improvement, product quality, site and compliance monitoring, staff resource planning, and staff and contractor performance management. • Provide support, expertise and represent project and clinical monitoring teams with sponsors/researchers throughout the project life cycle. • Ensure all team members, including third party providers, deliver high quality, timely service and maintain service delivery processes in accordance with corporate and industry best practices and that meet all regulatory requirements and guidelines.