Experienced Clinical Research Professional With 6 years of demonstrated experience in the Clinical Research industry, I bring a robust skill set in Project Management, Stakeholder Management, Site Payments, Clinical Monitoring, Risk-Based Quality Monitoring with robust systems experience like Electronic Data Capture (EDC), TMFs, Lab Supplies (LabCorp's Xcellerate), and IXRS (Calyx, Endpoint). My expertise spans Oncology, Immunology, Pulmonology, and Rare Disease Conditions across Phase 1 to Phase 4 Clinical Trials. I am certified in ICH-Good Clinical Practice (GCP), Stakeholder Management, and Budget and Finance Management. I possess a collaborative mindset and exceptional knowledge of working with research professionals and clinical trial sites (hospitals) across North and South America (USA, Canada, Brazil), Europe, and the APAC (Asia Pacific) regions. As a Subject Matter Expert (SME) for TMF, study close activities and archival, and safety distribution tools, I also mentor new hires, ensuring they are well-equipped to contribute effectively to our projects.