Areas of Expertise and Responsibilities
- Managing Director
- Clinical Trial Specialist (CTS)
- Certified Lead-Auditor
- Certified Commissioner for Data Protection
- Consultancy and Lecturing Activities
Study of pharmacy and training as information agent (DIMDI – German Institute for Medical Documentation and Information and DataStar Pharma Database). 1992 – 2000 deputy head of Regulatory Affairs department in an Austrian pharmaceutical company. Since 1996 active in the field of clinical studies as a clinical monitor, auditor and project manager. Certified Quality Lead Auditor and Quality Manager in Healthcare from the European Organization for Quality (EOQ), certified quality manager for medical devices and expert for regulatory affairs of medical devices from Quality Austria, as well as certified commissioner for data protection. Training as a “Clinical Trial Specialist” at the Medical University of Graz.