Our employees are selected from individuals who possess the necessary job values and have received education in life sciences or equivalent fields. Our current employees undergo training within designated time frames in accordance with current regulations, Good Clinical Practices guidelines, and study protocols.
• History of Clinical Research
• ICH - GCP Guidelines
• Local GCP Guide in Turkey
• Responsibilities of the Site Team
• Protocol, Visit Planning, and Visit Program Management
• Data Entry and Source Document Requirements
• Reporting Adverse and Serious Adverse Events
• Central Laboratory Procedures
• Patient Admission Procedures
• Management of Patient's Duration in the Study
• Management of Essential Documents
• Coordination with the Ministry of Health and Ethics Committee
• Communication Skills
• Time Management