Study management and reporting
Our operational team is the first point of contact between the sponsor and the investigation site. Our clinical project managers are experienced in phase I/II trial execution and implementation. They have a deep understanding of the specific project dynamics and study objectives, and supervise:
- SAE monitoring and follow-up;
- coordination of data management teams, bioanalytical laboratories and other partner’s activities;
- writing, coordination and review of clinical study reports;
- respect for study timelines and budget; and
- essential study document track records.