The coordinator supports the preparation of new studies and the optimisation of processes in the field of clinical research at the site as well as cross-site studies. Supervision of employees is as much a part of her job as quality management through the development, implementation and training of work instructions (SOPs) in your work area.
Our study physicians are in charge of the medical part of the studies. They inform the study participants about the studies, conduct anamnesis interviews, physical examinations, blood and nerve water sampling, skin biopsies and some of the cognitive tests.
|Dr. Friedemann Bender||friedemann.bender(at)dzne.de|
|Dr. Stefanie Hayer||stefanie.hayer(at)dzne.de|
|Dr. Anna Hofmann||anna.hofman(at)dzne.de|
|Dr. Christoph Keßler||christoph.kessler(at)dzne.de|
|Priv.-Doz. Dr. Matthias Munk||matthias.munk(at)dzne.de|
|Dr. Oliver Preische||oliver.preische(at)dzne.de|
|Dr. Carlo Wilke||carlo.wilke(at)dzne.de|
|Dr. Isabel Wurster||isabel.wurster(at)dzne.de|
Neuropsychology deals with the effects of brain diseases on cognitive and affective functional areas, which are mapped by means of standardised procedures.
The study assistants in clinical research primarily organise and coordinate the study-related procedures. This includes the collection (blood), first processing, storage and dispatch of biomaterial as well as the documentation of the collected data. The procedures are carried out according to standardised and carefully prepared work instructions (SOPs).