Clinical Trials

 

 

Services for Investigators

  • Assistance with protocol development
  • Routing grant proposals through appropriate channels at Dartmouth College
  • Determination of staff and financial resources required for completion of clinical study
  • Creation of data collection forms and computerized database
  • Assistance with writing informed consent
  • Submissions for IRB review
  • Clinical Cancer Review Committee for peer review of scientific merit of studies
  • Review of patient eligibility requirements
  • Patient registration system for inhouse protocols
  • Data collection and entry
  • Assistance with adherence to clinical protocol requirements
  • Coordination of investigational drug shipments and drug logs
  • Submission of adverse event reports
  • Safety and Data Monitoring Committee for review of inhouse studies
  • Subject follow-up