• Management of rare disease Clinical Development Teams (neurology, hematology, and nephrology)o Manages and maintains up to date project timelines inclusive of all critical milestones, deliverables, action items, budget, and key interdependencies by applying experienced project management techniques.o Coordinate regular clinical development team meetings including preparing the agenda, leading the meeting, writing and distributing minutes and ensuring action items are completed.o Coordinates yearly update of all Clinical Development Plans.o Ensures programs are properly resourced to meet objectives of global clinical initiatives.o Manage communication between team and senior management.• Utilize program management techniques to support successful planning and implementation of non-pipeline projects, such as development standard implementation and KPI tracking/reporting, as needed.• Supports inspection readiness activities.• Collaborates effectively and professionally in a highly cross matrixed environment.

• Coordinated and managed global ISS/ESC across the Dupixient respiratory portfolio.o Managed all ex-US studies from proposal submission through protocol review and coordinated study hand off to ISS Operations at the contracting stage.o Coordinated regular Scientific Review Committee meetings, which included: preparing the agenda, leading the meeting, writing, and distributing minutes and ensuring action items were completed.o Trained all new committee members on ISS voting with a focus on Sanofi best practices.o Regularly prepared and provided study metrics to senior leadership.o Worked closely with Global Medical Directors and senior management to provide status updates of the Dupixient respiratory ISS portfolio.o Alliance management with our partner company.o Acted as country medical teams’ main point of contact for review of new project proposals.o Regularly reviewed product portfolio to ensure adherence to timelines, addressed any delays to deliverables, and alleviated study related issues.• Liaised with global cross-functional team to develop annual Medical Plan.• Created and maintained an executive level dashboard for Dupixient highlighting key franchise activities across Medical Affairs.• Worked with key stakeholders to develop and maintain the Dupixient respiratory Annual Budgeting Plan (ABP).

• Early-Stage Program Managemento Managed content for and lead cross-functional project team meetings.o Created and maintained project timelines, meeting minutes, and agendas.o Worked closely with the finance department to manage project budgets.o Acted as primary point of contact for consultants.o Prepared RFPs and evaluated proposals from multiple preclinical CRO’s .• Assisted Head of Program Management with clinical-stage programo Acted as primary point of contact for consultants.o Facilitated cross-functional team meetings, generated agendas and meeting minutes.o Maintained an accurate and up to date timeline.o Worked closely with CMC to manage ongoing and future clinical supply needs.• Contract managemento Managed all contracting for the company, including but not limited to, CDAs, SRAs, MTAs, MSAs, consulting agreements and work orders for both clinical and preclinical work.o Experienced user of Conga Contracting Software.o Acted as primary point of contact between vendors/academic labs and the company.o Experienced in use of Microsoft Office Suite, including Project

Operations Management o Evaluated multiple compound and inventory management systems and presented recommendations to upper management.o Negotiated and maintained all service contracts on capital equipment.o Oversaw all laboratory purchasing, inventory and equipment maintenance.o Worked closely with finance to manage reagent spend at CRO’s.o Developed, implemented, and monitored laboratory protocols and best practices.o Organized the extensive compound library and developed a comprehensive, searchable document that allows compounds to be located rapidly.o Worked closely with safety consultants and various regulatory agencies to manage our permits and ensure the company remains in compliance.

• Utilized LC/MS/MS to generate high quality, quantitative compound exposure data for projects across discovery research.• Developed and validated an extraction and analysis protocol for the Mitra Microsampling System.• Trained in life staff across the company in proper microsampling technique.• Developed and validated LC/MS methods for biomarkers to aid program teams.• Member of a multi-disciplinary Continuous Process Improvement teamo Streamlined the process for requesting high throughput assays by evaluating multiple, commercial software systems and culminated with rolling out Biorails software to the entire research organization