Office of Clinical Research 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