Since joining the pharmaceutical industry in 2000, I have been actively involved in more then 20 international clinical trials. I have extensive experience in managing international projects as well as in setting up and monitoring sites in different therapeutic areas such as gastroenterology, hepatology, neurology, pain, dentistry and paediatrics. As a PM I was responsible for entire study management including vendor management, contracts and financial management of clinical trials. Since 2005 I am acting as a Country manager for Serbia and Regional Clinical Operational manger for the former Yugoslav republics. As a Clinical Operations manager I am responsible for a day to day support to Clinical teams in Serbia, Bosnia, Croatia, Macedonia and Slovenia and for coordination of cooperation between different departments on the local and the global level. I am also responsible for coordination of feasibility activities in Serbia and in the region. I am also involved in Business Development activities on the local and global level by attending Bid Defence meeting with clients and presentation during meeting with potential clients. I was responsible for quality control of operations in my region. I was also responsible for preparation and implementation of local SOPs, Clinical Operations and Regulatory Requirements (CORR) document for Serbia, Staff Handbook, Business Continuity Plans and Disaster Recovery plans for Serbia.As a Chairman of Serbian ACRP Chapter I am actively involved in setting up and improvement of clinical trials environment in Serbia. As a ACRP Certified GCP trainer I am involved in GCP training for Serbian Investigators and Clinical research professionals (around 6, three days training sessions per year).From January 2012 to July 2014 was acting as the Head of Education and Lecturer in CRA Academy, specialized 6 months long, training course for CRA (www.cro.rs) and other roles in CRO industry.Specialties: Feasibility, GCP training, CRA training