Clinical Services
Supporting your clinical research program. By teaming up with our Clinical Services team, you can reduce time to clinical trial activation while improving clinical research workflows.
Service Offerings
Research Site and Sponsor Relations
- Assessment of site clinical study readiness
- Assistance with trial sponsor contracts and budgets
- Scheduling sponsor site selection (site initiation visit [SIV] and site qualification visit [SQV])
Regulatory
- Training
- Regulatory forms
- Form submissions to sponsor, Institutional Review Board (IRB)
- Protocol management
- Pre-screening inclusion/exclusion checklist
- Standard operating procedure (SOP), subject matter expert (SME) support
Study Data Management
- Quality assurance and quality control (QA/QC)
- Patient pre-screening in electronic medical record (EMR)
Training
- Access to disease-specific training
- Access to best practices training
- Ensuring staff training is complete
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