Since 1990, I worked in the molecular diagnostic and pharmaceutical industry. During this period, I gained experience in research, marketing, project management, and regulatory affairs. Working in regulatory affairs, I have been involved in IND/IMPD registrations, MAA/BLA registrations and post-approval activities for Biotech products (e.g. recombinant proteins, antibody drug conjugates, vaccines) worldwide. I have also gained experience with quality, change control and compliance related issues. I am service oriented with an eye for detail and I think in possibilities and solutions. Starodub gives me the opportunity to work with client-oriented professionals that have different backgrounds and specialties and whose focus is to deliver timely and high-quality services.