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