We are proud to have highly qualified project managers and clinical research associates with university degrees in medical and life sciences. Our colleagues are continuously trained, up-to-date in local regulations and strictly adhering to the deadlines.

  • Project planning, tracking and reporting
  • Pro-active development of project-focused risk and mitigation strategies
  • Overall project supervision
  • Regular project meetings/teleconferences to review/plan the project scope, assumptions, timelines and activities
  • Primary contact with client/sites/vendors
  • Focused timelines and budget management
  • Preparation of weekly/monthly/quarterly status reports
  • Vendor management
  • Site payment management
  • Organization of investigators’ meetings
  • Initiation and activation of study sites
  • Remote monitoring
  • Risk-based monitoring
  • Regular site monitoring
  • Medical monitoring
  • Pharmacovigilance
  • Closing of study sites