Maria Lujan Martin

I am a healthcare professional transitioning into clinical research, with 9+ years of experience in clinical field operations, multi-site coordination, health indicator surveillance, and regulatory documentation at ACUMAR (Autoridad de Cuenca Matanza Riachuelo) in Buenos Aires, Argentina.

In July 2026, I completed a postgraduate certification in Clinical Trial Monitoring at FEFyM (Fundación de Estudios Farmacológicos y de Medicamentos), covering ICH-GCP E6(R3), ANMAT Disposición 7516/2025, Source Document Verification (SDV), Trial Master File (TMF) management, and Adverse Event (AE/SAE) reporting.

Throughout my career, I have:

- Expanded population health monitoring coverage by 350% — redesigning a data collection protocol to cover ~20,000 residents across 350 neighborhoods in 12 municipalities

- Maintained audit-ready documentation for 5 consecutive years with zero corrective actions, applying regulatory-grade QC standards equivalent to TMF and ICH-GCP requirements

- Coordinated stakeholder management across 12 municipal health centers and 3 government agencies simultaneously

- Supervised multidisciplinary field teams of up to 10 health professionals conducting systematic clinical biomarker monitoring (blood lead levels, vaccination coverage, glucose, cholesterol, child cognitive development)

I hold a degree in Hemotherapy and Immunohematology from Universidad de Buenos Aires (UBA, 2012), with hands-on experience in venipuncture, clinical laboratory, epidemiology, and infection control.

I am fluent in Spanish (native), English (professional proficiency), and Italian (intermediate). As an EU citizen (Italian passport), I am fully eligible to work across all EU member states without visa sponsorship and am open to relocation for CRA, CTA, or Site Management Associate roles.