Tiana Pavlidis

Director, Regulatory Affairs & Quality Assurance @Target Rwe

Establish and oversee the enterprise Quality Management System (QMS) supporting real-world evidence (RWE) studies, ensuring compliance with Good Clinical Practice guidelines, federal regulations, and applicable privacy and data use regulations- Partner with stakeholders to embed quality practices across functions, maintaining compliance with consent, privacy, and regulatory requirements- Lead enterprise-level compliance risk management by driving root cause investigations, implementing CAPAs, and embedding sustainable process improvement- Direct internal and vendor audit programs, developing risk-based audit plans, scoring matrices, and oversight frameworks to strengthen governance and accountability- Advance audit and inspection readiness by establishing proactive oversight frameworks, standardized documentation practices, and continuous quality monitoring- Implement enterprise systems for training compliance, SOP distribution, and project lifecycle tracking, ensuring organizational alignment and regulatory resilience- Serve as executive QA partner to Clinical Operations leadership, advancing deviation management, TMF compliance, and proactive inspection preparedness