Clinical * Hands on Experience in Monitoring of Clinical Investigations Study Initiation Study Monitoring Recruitment of Study subjects Study budget forecast and planning Retention of Study Subjects and Study Closeout procedures. * In depth understanding and training in the Review of the Study Protocol Processes and Procedures to ensure that all site personnel understand what is necessary to perform the study * Experience in all areas of research including budgeting GCP Ethics protocol submissions and safety reporting

Highlights:

• Management
• Monitoring
• Clinical Research
• Data Quality
• Forecasting
• Imaging
• Oncology
• Protocol
• Quality
• Quality Assurance