Head Of Clinical Trial Unit.
Current- arranging and conducting of clinical trials according GCP-regulation; - composing and/or expertise of clinical trals protocol; - choosing of base, auditing and contracting procedure; - applying for expertise and obtaining of regulatory approval of clinical trial; - monitoring of clinical trial;- composing and/or expertise of clinical trals report; - composing registration dossiers (CTD) (Module 2.4; 2.5; 2.6; 2.7; 4; 5). - arranging and conducting of preclinical studies according GLP regu-lation (bioscrining of specific activity of substances); - composing scientific articles (author of 21 articles), reports, speeches, conference arranging and participating; - ICH GCP certificate.