• Overall Clinical Trial Management

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

More Services

Overall Clinical Trial Management

Medical writing

Study feasibility

Regulatory services

Site & Investigator contract negotiation

Data management