Ruben Van Beers Email & Phone Number

I am a well-organized and results-oriented senior scientist with a solid scientific and technical background. I have over 20 years of experience in the pharmaceutical industry, mainly during late stage development of biotech products, including people management experience within my current role. I have knowledge of Regulatory Affairs basics and experience with supporting regulatory submissions and scientific writing. Study coordination, documentation management and quality aspects such as GMP, ICH guidelines, deviation and change management are an important part of my expertise.I work independently and I enjoy to be part of a multidisciplinary team as well. I want to be part of the organization to relate results with activities and I want to share my knowledge. By listening and remaining critical, I create solutions and a plan of action. I create structure in my activities in order to proceed efficiently with a pragmatic approach.--- team player | social | eager to learn | critical | focus on quality | eye for detail | structured | people management ---Expertises:study coordination | assistant project management | scientific writing | regulatory affairs and documentation | CMC | quality assurance | critical reagents

Listed skills include Technical Writing, Project Management, Gmp, Study Coordination, and 19 others.