Project Management, Monitoring

Quality work and strong leadership drive every aspect of our Project Managers' responsibilities. They are wholeheartedly committed to planning and directing clinical study projects to ensure compliance with standard operating procedures and a high-quality customer experience. To provide these outstanding results, our Project Managers rely on the loyalty and respect of their teams and build trusting relationships with all stakeholders to make sure that project needs are satisfied and expectations are surpassed.
As a matter of course all our Project Managers and CRAs are permanently trainend in SOPs as well as in current legal requirements and new developments.

What we do:

  • Feasibility
  • Site selection
  • Investigator recruitment
  • Identify appropriate vendor(s)
  • Select vendor in coordination with client
  • Negotiate the price and payment schedule
  • Pre-Study visits
  • Organisation and Conduct of Investigator meetings
  • Logistics
  • Initiation visits
  • Continuous status reports
  • Files handling
  • Management of Investigator's fee
  • Trial tracking in-house and at sites
  • SAE/SUSAR/AE reporting system
  • Trouble-shooting etc.
  • Telephone monitoring
  • Site-specific support
  • Source data verification
  • Query resolution
  • IMP accountability