Do you need a reliable and meticulous clinical research associate who motivates the study team?

You will find that with me!

  • Valid ICH-GCP certificate
  • Site Selection Visit
  • Pre-study-qualification visit
  • Site Initiation Visit
  • Site Monitoring Visit
  • Close Out Visit
  • Clinical Monitoring
  • Data Management
  • Organisation of Investigator Meetings/Trainings
  • Preparation and provision of regulatory documents
  • Query resolution
  • Preparation for audits and inspections