Greater Karlsruhe Area
Consulting on linical trials regulations and trial conduct Author and co-editor of textbooks on clinical trials
Manage and develop medcom’s core business of conducting clinical trials, project management and associated regulatory affairs; provide medical, scientific and regulatory input for clients and associates; ensure clinical trials are managed and conducted to current international standards; review trial documentation and data; provide services as a consultant; participate actively in the administration of clinical trials.
Clinical trials management and associated regulatory affairs, director of clinical investigation (LKP, Leiter der Klinischen Prüfung), scientific and GCP consulting for clinical trials Phase I to IV, PMS, medical communications, medical writing, translations, licensing; medical director, project leader.
Medical Communications
Marion Merrell Dow GmbH (MMD), Germany, and MMD Department of Clinical Research Strasbourg, France