Over the years I have gained a broad experience in clinical trials, thus becoming a truly all-round clinical research professional.
I have managed all types of projects: from small phase 1 trials to large global, phase IIIB, full-service programs, as well as investigator initiated trials. I have worked in several indications, but mostly cardiovascular.
Besides project- and line-management I have experience with many other aspects of clinical research such as: in-hospital trial coordination, site selection and start up, regulatory submissions, contracts & budgets, on-site monitoring, protocol & SOP development, database development, CRA training and coaching.
Currently I 'm available for new projects, so if you need support on any task, please contact me on firstname.lastname@example.org