Optimizing the technical readiness of digital assets for the MLR review cycle. With experience working on high-stakes pharma brands, I specialize in technical pre-flighting, Veeva-aligned UI architecture, and ensuring asset compliance before submission. I bridge the gap between design and PromoMats coordination, reducing rejection cycles through rigorous audit and operational clarity.
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.
Submission Workflow & Asset Coordination
Ensuring the operational reliability of multi-step patient and provider flows as they transition from design into the regulatory pipeline.
Focus: Managing system logic and asset lifecycle to reduce user error and ensure consistent performance across global Veeva Vault environments.
MLR Submission Readiness & Technical Pre-Flight
Managing the technical audit of complex form systems and structured data inputs to ensure high-density information is submission-ready.
Focus: Pre-flighting dosing and safety-reporting modules for PromoMats specifications to ensure field hierarchy and data integrity before legal review.
Regulatory UI Operations & Compliance Remediation
Streamlining the maintenance of state-driven interfaces and legacy UI debt to meet strict medical and legal standards.
Focus: Continuous WCAG 2.1/2.2 auditing and design system governance to prevent regulatory rejections and ensure long-term accessibility within the Veeva ecosystem.
