Cologne Bonn Region
Involvement in the entire process of running clinical trials: Country feasibility, submission to the regulatory authorities and the ethics committee, site selection, initiation, regular monitoring and site close out visits. I have experience from running clinical trials in Germany, Switzerland, Norway, Sweden and Denmark, phase II-IIII, and have trained site staff at study sites as well as internal staff. Therapeutic areas: Women's health (bacterial vaginosis, birth control), parkinson, migraine, vaccine (unblinded monitor), hepatit C virus infection, hemophilia, cardiovascular device-study diabetic nephropathie, uterine myoma and actinic keratosis. I am a diligent, ambitious and determined person who has an organized and analytical way of working. I’m proactive and responsible, and I’m eager to face new challenges where I can practice and further develop my skills. I work just as well independently as in a team, and I am social and amiable.
Clinical Research Associate. Outsourced to Bayer AS. Country Lead Monitor including budget responsibility.
Clinical Research Assistant: Aug 2007 - Aug 2008 Clinical Research Associate: Aug 2008 - Dec 2010 Organizing of Investigator Meetings, responsible for medication storage. Close cooperation with the QA-department (SOP updates).