Study Coordinator and Data Entry

We provide support in time-consuming activities, helping the research team to reach the Project deadlines on time with full quality assurance.

  • Clinical Trial Coordination: Our professionals are ready to support the research team, following its instructions and  delivering results on time.
  • Supporting the enrollment of subjects.
  • Transferring of study data to the CRF,  registering data and keeping updated all the research study tools.
  • Attending monitoring visits, participating in the visits scheduled by the CRA, helping to solve discrepancies.
  • Keeping updated the study files, such as Investigator Master File.
  • Dealing with regulatory requirements, acting as contact person or representative.
  • Writing and preparing all regulatory requirements before, during and at the end of the Study.