Site Management Services
Your Partner for
Site Management Organization
ClinPoint Trials can provide our range of centralized research skills to support your clinical trial site. From feasibility and site initiation to study completion and close-out procedures, let our 30+ years of cumulative research experience help your site conduct your study by minimizing deviations while maximizing data quality.
How We Can Help
- Contract / Budget Negotiations
- Institutional Review Board Management
- Clinical Trials Management System
- Study Protocol Management
- Regulatory / Compliance Support
- Study Participant Compliance & Follow-Up
- Adverse Event Reporting
- Study Close-Out Procedures
- Improved Overhead Costs
- Study Administrative Oversight
