Clinical Research Associate (CRA) and Clinical Trial Manager with extensive experience overseeing high-enrolling sites, ensuring compliance, patient safety, and data integrity. Skilled in site monitoring, site audits, and inspections, with a proven track record of successful results.Positive and dedicated to managing clinical trials from initiation through close-out, ensuring all trial phases are executed smoothly and in line with regulatory standards. Passionate about driving effective enrollment, safety, and data accuracy.As a Clinical Trial Manager, responsible for managing trial timelines, budgets, and resources. Experienced in training and mentoring site teams, leading cross-functional teams, and resolving site-related issues promptly to keep studies on track.Independent GCP auditor – conducted Investigator Site Audits in the EU, eTMF audits, and process audits (including RA and CEC submissions), ensuring all processes adhere to Good Clinical Practice standards.References available upon request.