I am a process optimization and automation professional with experience delivering AI-enabled workflows, enterprise reporting, audit-ready systems, and secure platform integrations across pharmaceutical and digital health operations.
I have built a career translating complex data, compliance, and operational requirements into scalable, production-ready solutions that improve efficiency and visibility for leadership teams.
In my current role as Product Manager – AI Center at MedStar Health, I lead process optimization, data management, and automation initiatives across telehealth, specialty consults, and enterprise platforms.
I have designed AI-driven document extraction workflows, developed executive-facing dashboards, and supported audit readiness and compliance efforts by coordinating with IS and Audit teams and helping define governance and acceptance criteria for enterprise AI deployment.
Previously, I operated my own consulting business and worked in IT project management and QC compliance at Regeneron Pharmaceuticals, where I managed dashboards, change management, drug-to-market campaigns, and cross-functional operational improvements.
My background includes hands-on experience with SharePoint, Power Automate, PowerApps, SQL, VBA, Jira, Confluence, and MS Project, along with a strong focus on automation, stakeholder coordination, and process improvement in regulated environments.
Led process optimization, data management, and automation initiatives across telehealth, specialty consults, and enterprise platforms. Designed and implemented AI-driven document extraction workflows, developed enterprise-ready dashboards and reporting solutions, and supported audit readiness and compliance efforts.
Maintained project-critical documents such as RAID logs, stakeholder registries, schedules, budgets, and impact reports. Led onboarding and implementation of IT applications and created RACI charts and supporting materials to improve operational clarity.
Created custom SQL KPI dashboards, coordinated relocation of four departments, and oversaw emergency FDA approvals for REGN-EB3 and Anti-SARS-CoV-2. Supported day 1 manufacturing compliance and QC procedures.
Created a custom SharePoint web part to streamline change management for drug-to-market campaigns. Improved communication and cadence processes, reducing review and writing times, and led a 3-person team recognized for top performance.
Led over 20 drug-to-market campaigns and managed remote and in-person teams under tight deadlines. Streamlined QC change management requests through PowerApps and automated change risk assessment documentation using VBA, improving completion speed and accuracy.
Bachelor of Science
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