The Easiest Way to Conduct Clinical Trials
Elligo Health Research’s End-to-End Research Support is a comprehensive research enablement program that provides new-to-research sites with everything they need to achieve Research Ready status and seamlessly conduct research going forward.
Offered exclusively through the Elligo Research Network, End-to-End Research Support helps:
Provide your patients with research as care
Reduce your administrative burden and overhead
Mitigate the risk associated with starting research
Increase your community visibility
Offer your staff comprehensive training
Customized Solutions to Make You Research Ready
End-to-End Research Support features personalized services to create a truly turnkey site:
Business Development
Connect with major pharma, biotech, device, and diagnostic companies to build a study pipeline.
Study Feasibility
Leverage electronic health record (EHR) data to match patients to studies and create accurate counts to present to sponsor partners.
Study Startup
Fully supported by Elligo project managers and regulatory teams.
Patient Recruitment
Optimized by a tech-enabled Patient Engagement team for both traditional and decentralized studies.
Budget Development & Contract Negotiation
Negotiate higher reimbursement and fast contract execution.
Study Coordination
Study-specific services to support ongoing activity.
Financial Management
Sponsor engagement and rapid payments.
No out-of-pocket payments to Elligo!
Introducing: IntElligo® Study Marketplace
Quickly and easily find and apply for studies that align with your interests, site capabilities, and patient population. Available soon to all Elligo Research Network members. Learn more.
Clinical Trial Support That Leaves You Free to Focus on Patient Care
| Description | RESPONSIBLE PARTNER | |||
| H/C Partner | Elligo | |||
Personnel |
Investigator | Overall responsibility for study conduct | ✔ | |
| Clinical Research Coordinator | Conducts most study processes locally | ✔ | ✔ | |
| CRC/Investigator Training | Credentialing for GCP and study | ✔ | ||
Functions |
Business Development | Identification of trials for site population | ✔ | |
| Feasibility | Achieve selection from sponsor on study | ✔ | ||
| Budget, Proposals, and Contracts | Negotiating optimal budget for site | ✔ | ||
| Regulatory | Submit regulatory documents to IRB | ✔ | ||
| Study Startup | Complete all startup procedures | ✔ | ||
| Patient ID, Engagement, and Outreach | Identify and recruit using EHR | ✔ | ✔ | |
| IntElligo® Use | Study workflow, eSource, and CTMS | ✔ | ✔ | |
| SOPs | Ensures compliance for audits | ✔ | ||
| On-Site Study Conduct | Assistance for surge or staff outage | ✔ | ✔ | |
| Regional Operations Support | Site Development Specialists to grow site | ✔ | ||
| Revenue Cycle | Manage receivables and payments | ✔ | ||
A Patient-Centric Approach to Clinical Trial Management
You know your patients. You understand what they need, what they care about, and how to best serve them in their healthcare journey — making the trusted patient-physician relationship integral to research success.
End-to-End Research Support is designed to maintain and augment this relationship, giving you the tools you need to participate in research so your patients have access to research as care in their community.
The Quickest Path to Becoming a Clinical Trial Physician
When you partner with Elligo to establish your research practice, you could be conducting clinical trials in just six weeks!
Research Ready in Four Simple Steps
- Confirmed interest from all practice stakeholders
- Needs and Readiness Assessment online form and a facility tour to determine needs and capabilities
- Practice Collaboration Agreement and Business Associate Agreement to formalize the partnership
- Onboarding and training
