NERI offers clinical research services for trials and registries from start-up through study close-out.
| Study Start-Up Subject EnrollmentStudy Close-Out |
- Protocol Design
- Site Selection
- Regulatory Strategy
- IRB Submission
- CRF Creation
- Database Setup
|
- Randomization
- Site Management
- Site Training
- Clinical Monitoring
- Tracking Data and Queries
- Biological Sample
Tracking
- Core Imaging / Adjudication and
Data Transfer
|
- Data Cleaning
- Database Lock
- Final Analyses
- CSR Compilation
- Regulatory Submissions
- Publication Support
|
NERI has been conducting clinical research since it was founded in 1986. This experience, along with a large staff holding diverse skill sets, allows NERI to create the best team for any particular client project.
Upon project initiation, a single project manager is assigned and is accountable to the client. Our goal is complete transparency to the client from start to finish. A standard set of study metrics and a project-specific timelines are agreed upon upfront to ensure accountability throughout the trial duration. Unlike other CROs, NERI’s key team members are typically assigned only 1 or 2 projects at a time, which allows them to focus intently on achieving project goals in a timely and cost-effective manner. Staff member skills are enhanced with rigorous training in project management, human subjects protection, and Good Clinical Practices.
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