Study Coordinators

All of SMO-Pharmina’s coordinators have medical education, experience of participating in different phases of clinical trials, and are fluent in English.

The Coordinators join the study teams and support the Investigators in all the activities necessary for conducting clinical trials effectively. As a result of close cooperation with the study team, coordinators:

  • Plan patient visits,
  • Complete eCRF according to source documents accurately and timely
  • Update site files on a regular basis
  • Manage IP-related procedures
  • Ensure correct collection and processing of biological samples
  • Ensure effective communication among all parties involved in the study

The Study coordinator’s involvement makes it easy for the study team to work and the sponsor is guaranteed to receive data accurately and on time.