While the CTC can provide complete study coordination to an investigator, they can also provide any one of a range of services including, but not limited to: 

  • Site selection and feasibility assessment
  • Budget development and negotiation, facilitate contract negotiations and execution, financial billing compliance approval , financial tracking and management
  • Logistical considerations and planning, study start up and staff training
  • IRB Preparation and submission,  IRB amendments, adverse events, annual reviews
  • Regulatory document compilation and maintenance  (FDA approval of INDs and IDEs, Medicare billing approval)
  • Design of Source documents and Case report forms
  • Patient Recruitment, Screening, Consenting and Follow Up
  • Drug administration, dispensing and accountability
  • Phlebotomy and specimen processing and storage
  • Data management services (data collection, data entry, internal QA/QI audit program)
  • Study close out and archive