Kimberly Matus Email and Phone Number

• Clinical Supply Operations point of contact, with Supply Chain Leads and Clinical Research Pharmacists, for the design and implementation of program and study level clinical supply operational strategies• Accountable for mid-to long-term supply chain strategies in support of execution of assigned programs and initiatives that include forecast and coordination for key packaging, labelling, distribution, and logistics events; ensure compliance with all legal requirements (e.g., EHS, cGMP, GCP, import/export, Quality Standards, 21 CFR Part 11) • Monitor the effectiveness of the operational strategies and partnering with functional line leads in Clinical Supply Operations (CSO) to ensure seamless implementation of operational strategies and delivery of clinical supplies• Develop robust packaging and distribution/ logistics planning and management tools; optimize operational strategy to ensure patient continuity; high quality project oversight and activity review• Manage/lead the enhancement of Clinical Supply Operations interface with clinical supply systems

• Lead and coordinate development of innovative solutions to enhance clinical supply chain by reducing cycle time and resources for clinical packaging using Robotic Process Automation technology• Lead cross-functional project teams to assemble business requirements, manage the system validation process, and ensure business needs are delivered on time, on budget and with superior quality for internal ISO system development, enhancements and integrations• Oversee Waterfall and Agile software development processes for clinical supply packaging and distribution systems for on time delivery of strategic deliverables• Contribute to the design and implementation for replacement of legacy clinical supply systems as system SME• Collaborate with Clinical Research Pharmacy and Mobile Digital to define the Mobile Strategy for the Impala Kit Verify Mobile application enhancements and adoption • Serve as the ISO Representative on the QTS Compliance Forum; monitor and ensure quality and compliance for on-time closure of ISO quality tracking records

• Led data migration for ERP system implementation for Clinical Packaging • Led and coordinated technical and system-related activities within the Supply Chain Business Support (SCBS) team• Provided business representation for clinical supply information systems used by Global Clinical Supply and their customers • Coordinated key activities including global business system administration, troubleshooting, reporting, end-user support, training, inspection readiness and regulatory compliance• Interfaced closely with system users, other SCBS staff, Digital, Quality Assurance (QA) and internal/external vendors that support key applications• Led and participated on small to large scale cross-functional project teams to assemble business requirements, manage the system validation process, and ensure business needs are delivered on time, on budget and with superior quality• Oversaw waterfall style software development lifecycle of Clinical Supply Distribution System (CSDS), Pfizer’s primary clinical supply distribution technology

• Developed strategies and established workflows to seamlessly enable integrated sourcing paradigm at CRO locations based in Shanghai• Designed and implemented integrated inventory and supply chain infrastructure at CRO site located in Shanghai China to support Pfizer Research from compound synthesis to assay screen (at external CROs and Pfizer)• Responsible vendor relationship management of Pfizer’s Global Neat Compound Repository, Liquid Repository/Sample Logistics (Shanghai, China), and logistics activities at CRO screening partners located in China, Europe and United States• Collaborated with Pfizer Technology Lines, Chemistry and Research Units to create and implement workflows and logistics paths to reduce screening cycle times by 42% from compound registration to screen • Global Business Lead and support for CART (Compound and Assay Request Tool); Responsible for Global roll-out and training of the CART request application. Provided support to Pfizer Project Teams, CRO’s, Chemistry, and Pfizer Technology Lines • Managed a team of Business and Research Operations project managers: managed materials tracking, logistics, and departmental resources and financials• Active member on the External Research Search Solutions Leadership Team to set and implement external research strategies and active participant on multiple cross discipline limited duration teams

• Managed client portfolio in excess of $150MM consisting of 25 diverse research client groups spanning from biopharma, small and large pharma, commercial research, and government agencies • Ensured smooth and efficient compound supply chain to client groups in a variety of formats; ensured services were delivered on time and within budget• Responsible for all Compound Management Projects and Informatics development at the San Francisco site; implement timelines, budgets, procedures, staffing requirements, and resources• Directed and coordinated the project management and informatics activities: ensured client satisfaction; accomplish project goals and objectives on time while meeting revenue, margin, and budget targets• Established data storage and exchanged protocols that meet client business requirements• Partnered with Business Development to attract new business partners; prepared responses to proposals and schedules of work for commercial, not for profit, and government agencies• Managed a team of project managers, informatics developers, and business analysts • Active member on the Compound Focus Leadership Team to set and implement business strategy

• Established, guided, and coordinated execution of informatics strategy to enable R&D outsourcing initiatives for chemistry, biology, supply chain, PDM and AMDE• Support supply chain logistics for integrated sourcing initiatives for CRO collaborations: Set overall compound logistic strategy (supply chain/data transfer) that met the needs of outsourced work, decreased in timelines, and increased cost efficiency• Monitored external collaborations and ensured compliance to contracted standards• Established infrastructure to process, transfer and consolidate solid sample inventory from 6 Pfizer sites to outsourced establishment with minimal impact to compound availability for research; effectively managed 6 site sample repositories during inventory transitions, personnel attrition, and site repository closures• Managed external partnerships and corporate assets of the non-GMP Solid Sample Repository in excess of 3MM samples for global distribution to Pfizer sites, external partners, universities, external research; monitor and ensure contractual obligations are met• Coordinated infrastructure for networking and communication for data integration between Pfizer and off-shore external partners (CROs): secure communication, data upload and integration• Evaluated CROs for outsourced partnerships; establish terms and contracts• Effectively forecasted departmental spend; manage, track budgets in excess $15MM• Active member on the External Research Search Solutions Leadership Team

• Managed diverse department consisting of management, scientific, technical, and contract staff in support of inventory control, data and process management, production and distribution of proprietary compounds, commercial chemicals and DEA controlled substances• Responsible for inventory and data management of four repositories (1MM+ samples) consisting of proprietary compounds (neat/liquid), commercial chemicals and regulated/controlled substances • Developed and implemented processes to ensure prompt registration and integration of compound libraries acquired through company mergers and acquisitions• Designed and implemented a centralized liquid sample distribution facility and processes that facilitated the transition of compounds from synthesis and purification to screen. Implementation reduced overall costs by 85% • Acted as a liaison between Pfizer Material Management and outsourcing companies for compound/chemical procurement, transfers, receipt, and registration of monomers and chemical libraries

• Supervised technical and contracted Surplus Chemical Stockroom staff. Daily duties included supervision and process management: stockroom inventory maintenance, compound dispensation, distribution, and registration. • Implemented processes and executed the sourcing, procurement, tracking, registration, integration and re-supply of HSA fragments, monomers, and fragment library collections• Designed and implemented a chemical inventory system that improved stockroom efficiencies by 50%, enabled accurate, real-time inventory data and provided electronic chemical inventory audit trails• Developed and implemented a method to source, track, receive, transfer, and register compounds sequestered for HSA Fragment Library replenishment• Act as a chemical sourcing and procurement agent to locate suppliers for chemical libraries. Procured and sourced an excess of 12,000 compounds for the Fragment chemical library