Clinical trial management

Tasks at a glance

• Coordination of studies (resource planning)
• Support with study design and ethics applications
• Preparation of documentation
• Creation of documentation systems
• Organization of the study outpatient clinic / scheduling appointments for patients
• Documentation of data
• Support with the evaluation of X-ray images
• Support with statistical analysis

Contact

Dipl.-Dok. (FH) Yvonne Noll, M. Sc.
Phone: +49 (0)511 5354 649
Fax: +49 (0)511 5354 873
E-mail: yvonne.noll(at)diakovere.de