Clinical Trial Site Management
Manage Your Study for Optimal Performance and Timely Results
GBC practices adaptive study management and works with sponsors to manage study sites and logistics to meet enrollment or testing goals and timelines. GBC offers solutions to customize and streamline processes for identifying, screening, and enrolling patients. GBC clinical trial site management services include:
Management of Clinical Sites
- Maintain Knowledge and Oversight of Clinical Site Operations
- Develop Supportive Relationships with Principal Investigators (PIs) and Clinical Research Coordinators (CRCs)
- Answer Specific Study Related Questions
- Coordinate Clinical Site Feedback and Communications
- Regularly Compile and Report Clinical Site Performance Metrics
- Track Study Site Milestones Including First-patient-in (FPI), Last-patient-in (LPI), Last-patient-out (LPO)
Management of Specialty Labs (Central Labs)
- Instrument Install and De-Install Services
- Support for Installation Qualification (IQ), Operational Qualification (OQ), and Performance Qualification (PQ)
Management of Third-Party Vendors
- Clinical Research Organizations (CROs)
- Site Management Organizations (SMOs)
- Contract Diagnostics Organizations (CDOs)
- Clinical Data Management Providers
- External Biorepository Facilities
- Production and Manufacturing Facilities
- Packaging Facilities
- Supply and Logistics Vendors
Clinical Study Financial Management
- Maintain Real-Time Financial Oversight
- Review Invoices and Reconcile Trial Expenses
- Track Milestone Payments
- Track Bonuses and Incentives
- Track Compliance Results and Overall Completeness
For additional information on GBC's clinical trial services please contact trials@globalbioclinical.com or register and send us your inquiry here.