Clinical Development Starts At Trial Site
Trials Hub integrates the clinical trial model as a business by crafting subject enrollment procedures, operational workflows and quality management processes that oversee study startup, execution and closeout.Our approach to performance results in more subjects enrolled, fewer dropouts and higher data quality.
Solutions We Offer
At Trials Hub, we help physicians successfully match, and set up the research infrastructure required to actualize successful clinical trial outcomes.
- Study Matching – We do the legwork to find studies appropriate for your patient populations. We go beyond by ensuring that your site and staff are prepared – at no cost to you.
- Contract & Budget Negotiation – We negotiate budgets, and create profitability models to ensure the study is executable, and generate a surplus for your medical institution.
- Study Oversight – We oversee study operations from study startup to closeout. This includes IRB submissions, regulatory document management, recruitment and quality management.
Our Solutions Include:
- Study Selection and Startup
- Vendor Selection and Oversight
- Filling out SFQs
- Handling contracts like CTA & CDA
- Budget Negotiation
- Maintain Invoices
- Sites Submissions for IRB
- Assist Sites with Regulatory Packages
- Assist Sites with Visits: SIV, MV, and Close-out
- eReg Binder Management
- Developing eLearning / Remote Training for SIV
- eCRF Design
- Clinical Project Management
- Remote and Risk-Based Monitoring
- Data Management and Queries
- Quality Assurance
- Payment Reconciliation