Operational management of clinical trial sites in Francophone Africa
AFCRA acts as an SMO by supporting investigation sites in the organization, coordination and operational execution of clinical trials, in close collaboration with Sponsors and CROs.
Site Management consists of to manage and structure the activities of the investigation site in order to ensure the execution of clinical trials fluid, compliant and efficient, throughout the entire study cycle.
Sponsors
CROs
Investigation sites
🏦 Sponsors & CROs
- ✅ Fewer fragile or underperforming websites
- ✅ Clear visibility on progress, quality and recruitment
- ✅ A single local operational contact for multiple sites
🏥 Investigation sites
- ✅ Concrete support for structuring clinical research activity
- ✅ Assistance with team organization, documentation, and processes
- ✅ Increased autonomy and credibility with sponsors
Better organized sites
More structured, more responsive, and better-prepared research sites to host studies.
Reduced operational risks
Significant reduction in quality discrepancies, delays and documentary non-conformities.
Better quality of workmanship
Better quality data, better adherence to protocol, key indicators monitored in real time.
Smooth communication
Structured and efficient interface between sites and project teams, Sponsors and CROs.
Clinical Research Training
Practical training adapted to the French-speaking African context.
Availability & Opportunities
Qualified resources mobilized according to your field needs.
Need on-the-ground operational management for your clinical trials?
Contact us to discuss your needs and define a suitable support plan.