Eric Rachev

Background

About Eric Rachev

With over nine years of experience in clinical research, I possess a strong understanding of regulatory requirements including GCP and ICH guidelines, as well as trial and site initiation and closure processes. I am proficient in the use of various clinical trial management systems and have a demonstrated ability to exercise effective decision-making. In my experience I served as a knowledge holder and active SME for the client's IRT and Integrated Drug Release platforms, collaborating with the client and the clinical trial team during trial initiation and trial closure phases. My leadership and coaching skills enable me to maintain effective working relationships with colleagues, managers, and clients. I am reliable and professional with excellent time management and organizational skills.