We choose our personnel from individuals educated at faculty of science and letters and who have business values. To train expert staff in the field, SMO Lead supports personnels with site training and teorical training.
We train our staff for appropiate, in timely manner reporting according to GCP regulations and protocol of trials approved from health department.
Our main training topics are;
- History of Clinical Trial
- ICH-GCP
- Turkish GCP
- Roles and Responsibilities of Site Staff
- Protocol, Visit scheduling and Visit Procedures Management
- Data Entry and Source Document Requirements
- Adverse Event/Serious Adverse Event Reporting
- Central Laboratory Procedures
- Subject Reimbursement Procedures
- Fraud and Misconduct
- Essential Documents Management
- MOH/Ethics Committee Coordination
- Communication Skills
- Time Management