Site Management

• Creating And Updating Patient Database
• Placing trained and qualified CRC at the site
• Identifying Patients As Per Study Requirements
• Assist In ICF And Screening Process
• Coordinate And Conduct All Visits According To The Protocol
• Clean And Accurate Data
• CRF Completion With In Agreed Timelines
• Training The Study Staff With Respect To Protocol And Study Procedures
• Investigational Product Storage, Dispensing And Accountability
• Maintain Site Master Files
• Updating All Logs
• AE/SAE Reporting And Follow Up In A Timely Manner
• Assist Site Close Out
• Record Retention
• Data Archival