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Home > RSO Services
RSO Services
Industry relations
Single source access to clinical and basic researchers
Site management--identify investigators, identify study sites, identify/locate study subjects, track study performance
Access to database of AHC investigators, equipment, technologies, and research subjects
Promote development of AHC technology
Identify and secure grants for AHC investigators
Investigator services
Study Start-up (clinical trials and basic research)
- Initial consultation (protocol review)
- Budget preparation
- Contract negotiation
- Approval process (prepare and submit IRB, IACUC, DHES, conflict management review, legal, Sponsored Projects Administration, and regulatory [FDA 1572] documents )
Study Conduct (clinical trials)
- Provide study coordinator (Clinical Research Coordinator)
- Train study coordinators
- Train investigators
- Assist study subject recruitment
- Track subject accrual
- Administer drugs, sample blood, monitor patients
- Complete case report forms (CRFs)
- Review investigator/coordinator performance
- Report serious adverse events (SAEs)
- Manage project finances
- Manage regulatory compliance
- Process protocol amendments
- Submit final reports
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