Medical Monitoring

Trionfo Research's medical monitors come from diverse therapeutic backgrounds, bringing the clinical and research expertise necessary to provide rigorous medical oversight of clinical trials. Our medical monitors offer a range of services tailored to the needs of each trial, including:

  • Providing input into the study protocol, informed consent forms, and project risk assessment
  • Training investigational sites and study teams
  • Supporting investigational sites with queries regarding eligibility, safety, etc.
  • Reviewing serious adverse events (SAEs), coding SAEs, and writing safety narratives
  • Reviewing patient data to identify trends and risks across the study

Our medical monitors are regionally located to provide complete coverage for investigational sites in various time zones. This localization enables effective communication in the local language and a familiarity with local clinical practices and culture, which helps foster stronger ties with investigational sites and study teams.
At Trionfo Research, our medical monitors provide rigorous medical oversight from the design phase to delivery, ensuring that your clinical trials are conducted with the highest standards of quality and compliance.