EARLY - PHASE CLINICAL RESEARCH
Based in the European Union, fully GCP compliant, with a dedicated Phase I unit of up to 72+ participants.

TMF Specialist & Site Operations Expert while also assisting in business development and projects. 5+ Years of experience in clinical research
Meet our core team of experts at CRS d.o.o., who have been with us from our beginnings.
Founder & CEO of CRS, Leading and supporting clinical operations in region. Tanja has more than 25 years of experience in clinical research.
Co-founder and senior expert in EDC systems and clinical data validation, with more than 25 years of experience ensuring data integrity across clinical studies.
Experienced in study coordination, site and subject oversight, visit tracking, eCRF design, data validation, and end-to-end clinical data operations.
Provides medical safety oversight, including AE/SAE review and GCP-compliant safety reporting across clinical studies.
Leads clinical studies in pulmonology with a focus on subject safety, protocol compliance, and data quality.
Conducts clinical studies from screening to completion, ensuring high-quality data and patient safety.