• Lead Clinical Development & Operations projects to elevate clinical and statistical business processes and workstreams.• Responsible for providing deep subject matter expertise and leadership in the delivery and management of Research & Development solutions.• Management Point of Contact (POC) for mapping, planning, and integration of content for newly in-scope business areas, acquisitions, collaborations, and divestitures.• Develop strategic technology roadmaps, budgets, and project prioritizations across diverse organizational stakeholder groups.• Support compliance activities for internal and external audits, interfacing with company and agency inspection professionals.

• Lead business analysis teams in the ideation and delivery of top clinical projects• Establish relationships with clinical business partners and members of technical project teams and liaise between customers and technical colleagues, aligning needs across various organization levels.• Develop business analysis management plans, work breakdown structures, project scopes, and development roll-out strategies for clinical projects. • Collaborate with Information Management teams, providing input on change management and business readiness strategies and identifying process improvement opportunities. • Oversee and coordinate project management and vendor activities, where appropriate, to ensure proper resource management and compliance with Pfizer's Solution Delivery Lifecycle (SDLC) protocols.• Lead initiatives to ensure high-quality standards for business analysis deliverables and requirements collection in agile project teams. • Present and communicate key aspects of project execution and milestones to project team members, leadership teams, and sponsors. • Identify issues and raise risks to project teams and assess the potential impact on budget or change in project scope.

• Supported data workflow and curation needs, external data integration, and enabling biology data capture in support of strategic collaborations with external partners.• Provided scientific domain knowledge, technical insight, and data workflow expertise for corporate data repositories.• Acted as a subject matter expert and liaison between research scientists and technical teams to effectively communicate challenges identified within the business and develop strategies to implement digital solutions.• Enabled support for the pharmacology data portfolio, including protocol registration, application template development, data publication processes, and application issue resolution. • Participated in application releases by providing testing support, script creation and review, and subject matter expertise for technical teams. • Worked with key business partners to create and deliver training documentation as needed to support product updates and releases.

• Lead the development and optimization of primary and secondary plate-based phenotypic assays in Pfizer's High Content and Flow Cytometry Primary Pharmacology group.• Provided weekly screening status reports to deliver high-quality, decision-making pharmacology data, supporting projects in multiple therapeutic areas.• Managed external assays and data generated by external CROs while simultaneously coordinating with chemistry and compound management groups to deliver screening compounds subsets of interest. • Worked with project team members to manage weekly screening schedules and develop individual studies to further investigate targeted biology (i.e., automated time course experiments and specialize phenotypic screening of novel treatments for Cystic Fibrosis and Sickle Cell Anemia).• Publications: SLAS Discovery- High-Throughput Surface Liquid Absorption and Secretion Assays to Identify F508del CFTR Correctors Using Patient Primary Airway Epithelial Cultures

• Interfaced with the laboratory scientists as a primary point of contact for the technical and logistical aspects of processing, storage, and global distribution of bio-fluid samples. • Worked collaboratively with laboratory support contractors, informatics teams, and scientists to meet department goals and Pfizer's strategic and operational goals. • Ensured compliance with Pfizer standards by following and authoring standard operating procedures (SOPs) to process biological specimens using robotic and automated systems. • Monitored, documented, and tracked all automated and manual handling of bio-specimens through the BioBank Specimen Management Systems (BSMS).• Coordinated with clinical research study teams and external CROs to receive and maintain an inventory of biological specimens and ensure the quality and organization of reserved, banked, and ordered samples.

• Participated in independent research in conjunction with the University of Wisconsin, La Crosse, and the Gunderson Lutheran Healthcare System, conducting cell-based assays on cultured human lymphocytes to explore the immunosuppressant properties of novel fungal metabolites on cytokine production• Awards and accomplishments: National Science Foundation S-STEM Scholarship Winner (2007-2011) and Outstanding Student Presentation Award Winner – Seven Rivers Undergraduate Research Symposium (2010)