I am a Clinical Research Coordinator and Project Manager with solid experience leading complex clinical trials and research programs across multiple therapeutic areas. I have coordinated more than 100 studies, including Horizon Europe and H2020 consortia, developing a strong foundation in operational strategy, regulatory compliance, and cross‑functional project execution.

My work focuses on end‑to‑end project management: workflow design, milestone oversight, risk assessment, and coordination between clinical, regulatory, and data teams. I manage data processes with precision — from dataset structuring and cleaning to biostatistical analysis using SPSS, R, Jamovi, JASP, and Excel. I prepare high‑quality documentation, including protocols, IRB submissions, SOPs, databases (SharePoint, REDCap, OpenClinica), statistical outputs, and manuscripts for peer‑reviewed journals, ensuring consistency, traceability, and rigorous version control.

I hold a Master’s in Clinical Trial Monitoring and am currently completing a Master’s in Biostatistics. My background includes deep knowledge of EMA, MDR, and GCP frameworks, hands‑on experience across phases I–IV, and certification by BSI Group in MDR technical documentation. I am experienced in drafting clinical trial protocols, clinical investigation plans, and regulatory documentation, and I work fluently with reference management tools such as Mendeley and Zotero.

Previously, as Head of R&D in a company operating more than 20 clinics conducting clinical trials simultaneously, I developed the ability to manage multiple high‑impact projects in parallel, transforming operational complexity into structured, efficient, and reliable processes. I am recognized for my analytical mindset, strong scientific writing, and consistent delivery of high‑quality results in demanding environments.