Regulated Asset Readiness & UI Operations for Pharma Teams
Helping pharma teams get digital assets compliance-ready before they hit the review cycle. With 4+ years on high-stakes pharma brands, I specialize in technical pre-flighting, MLR-adjacent workflow support, and ensuring HCP-facing interfaces meet regulatory and accessibility standards, bridging the gap between creative delivery and regulatory handoff.
B2B Experience
Projects
ULTOMIRIS®
Regulated UI Operations & Clinical Workflow Maintenance
Sunosi
Regulated UI Operations & Clinical Workflow Maintenance
Disclaimer: The work shown was completed during full-time employment and is shared to highlight my role and contributions. These are not clients of Stone Interface.
Regulated Asset Handoff & Workflow Coordination
Supporting the operational reliability of multi-step provider and patient flows as they move from design into the regulatory review pipeline.
Focus: Managing asset lifecycle, component logic, and handoff documentation to reduce friction and ensure consistency across compliance-driven review cycles.
MLR-Adjacent Pre-Flight & Technical QC
Conducting technical audits of complex interface systems and structured content to ensure accuracy and completeness before regulatory review.
Focus: Pre-flighting dosing modules, ISI placement, and safety-reporting components against regulatory specifications to support data integrity ahead of legal and medical review.
Accessibility Compliance & Regulatory UI Remediation
Maintaining and remediating state-driven interfaces and legacy UI to meet strict medical, legal, and accessibility standards.
Focus: Continuous WCAG 2.1/2.2 auditing and design system governance to prevent compliance gaps and ensure long-term accessibility within regulated environments.
