Tibor Czégeni

Additional duties beside the ongoing Clinical Research Coordinator tasks:

• Being the main contact person between the PIs, sponsors, CROs and vendors
• Conducting monitoring visits and meetings with CRAs
• Feasibility and study start-up/closure procedures
• Maintenance of the Trial Master Files
• Communicating with the Local Ethics Committee
• Writing SOPs for the investigative team
• Working on contracts with the lawyer
• Budget planning and writing financial reports
• Participating in international investigators meetings

On-site management of gastroenterology-related clinical trials (Phase II and III.):

• Reviewing medical histories according to inclusion and exclusion criteria
• Coordination and documentation of patient visits
• Updating patient data in eCRF and query resolution
• Participating in endoscopic procedures and handling biopsies
• Preparation and shipping of biological samples
• Ensuring continuous lab kit and equipment supply

Main responsibilities at the Department of Gastroenterology and Oncology:

• Summarizing medical histories and writing anamnesis
• Consulting about cases and therapies with physicians, biologists and dietitian colleagues
• Performing vital parameter and body composition (BIA) measurements
• Installing Continuous Glucose Monitors (CGM)
• Informing patients about prescribed therapies
• Explaining nutritional therapy protocols for patients