15 years in clinical research in CRO industry. 11 years of experience in conducting GCP audits on investigational sites, Trial Master File audits, system audits, vendor audits and sponsor audits. Audits conducted in Russia, Ukraine, Belarus, Poland, Serbia, Romania, Baltic countries, Germany, Italy, India, Chroatia, etc. 4 years of experience as CRA in clinical trial qualification, initiation and monitoring of investigational sites with emphasis on compliance with local requirements, GCP and SOPs of international studies in urology, oncology, pulmonology. I have worked for PAREXEL for almost 6 years, following 6 years in another CRO. I started my career as CRA then moved to QA Department. I joined PAREXEL as an Auditor II.
Pulmonology