Our Mission
To expand access to clinical research by empowering community physician practices with the tools, expertise, and support needed to successfully participate in clinical trials- and to help sponsors and CROs connect with high-quality, diverse research sites.
Our Departments
Our Specialized departments work together to prepare, support, and connect research sites with study opportunities
Contracts & Regulatory Team
Supporting compliant, efficient study start-up and ongoing regulatory management.
CDA, CTA and contract coordination
Budget review and negotiation support
Regulatory document collection and maintenance
IRB submission and activation support
Investigator Site File documentation
Ongoing regulatory compliance and study updates
Site Project Management Team
Coordinating the operational pieces that keep sites and studies moving forward.
Site onboarding and research program setup
Study start-up and activation coordination
Site readiness and equipment oversight
Staff training and delegation support
Vendor and study-team coordination
Recruitment and study execution support
Monitoring preparation and ongoing site management
Central point of contact throughout the study lifecycle
Data, Quality Support Team
Strengthening site readiness, data quality, and research compliance.
5-Star Site Readiness Reviews
EMR data mining and patient-population analysis
Feasibility and enrollment assessments
Source-document and documentation quality support
SOP and workflow development
Quality reviews and corrective-action support
Monitoring, audit, and inspection readiness
Ongoing quality and compliance oversight
Business Development Team
Connecting the right investigators and patient populations with the right study opportunities.
Sponsor and CRO outreach
Study opportunity identification
Investigator and site positioning
Site profile development
Therapeutic-area and patient-population matching
Feasibility opportunity coordination
Sponsor/CRO relationship development
Pipeline management and follow-up