Office of Clinical Research Services
- 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 data base
- Assistance with writing informed consent
- Review of patient eligibility
- Patient registration system for in-house protocols
- Data collection
- Assistance with adherence to clinical protocol requirements
- Coordination of investigational drug shipments and drug logs
- Submission of adverse event reports
- Data entry
- Patient follow-up
- Submissions for IRB review
- Clinical Cancer Review Committee for peer review of scientific merit of in-house studies
- Safety and Data Monitoring Committee for review of in-house studies
- Gateway to clinical trials research network comprising many rural hospitals throughout northern New England.
