Shared Resources

 

 

Service Process

  1. Notify OCR, disease specific, Clinical Research Coordinator or Administrative Director (OCR general number 603-653-9071) when a new clinical trial is being proposed.
  2. Assistance is available for all steps of opening clinical trials including investigator initiated, federal, and industry sponsored trials. Confidentiality agreements (CDA), contracts, and budgets are negotiated through the Clinical Trials Office (CTO).
  3. CRCs and regulatory specialists provide complete services (prior to opening a study through close out of a study) including IRB submission, submission and maintenance of regulatory documents and participant data, coordination with sponsors for site initiation, monitoring, and investigational pharmacy visits. OCR staff work with CTO, CPHS, and sponsors on all aspects of a trial. CRCs and regulatory Specialists provide complete services (from protocol concept to close of a study).
  4. Research Nurses serve as the clinical liaison to assist with informed consent, symptom management, and clinical conduct of the study.