Bringing over 8 years of expertise in overseeing operations in Cardiovascular, Renal, Metabolism (CVRM), and Oncology trials (Phase 1-3). I build and sustain impactful partnerships with key opinion leaders (KOLs), sponsors, and stakeholders across academic research centers, hospitals, and CROs to achieve outstanding results.I direct the full lifecycle of clinical trials for medicines and biologics—upholding the highest standards in quality, timelines, and productivity to advance patient care.Core Competencies* Study Design, Protocol Development* Site Selection, Feasibility * Regulatory Compliance (ICH-GCP, FDA, EMA)* Clinical Trial Operations * Risk-Based Monitoring* Investigational Product Management (IMP)* Site Training, Monitoring* Patient Safety Reporting* Data Integrity, Documentation* Stakeholder Collaboration