Solutions Research Group is a premier clinical research network dedicated to connecting pharmaceutical sponsors, principal investigators, and diverse patient populations to drive medical innovation safely and efficiently.
Operational benchmarks that sponsors and CROs can hold us to, from regulatory turnaround to audit-ready trial binders.
Accelerated central IRB reliance, swift budget/CTA negotiation, and reduced cycle time to First Patient In (FPI).
Proactive patient engagement, automated visit reminders, and dedicated CRC support to minimize dropouts.
Full ICH-GCP compliant workflows, double-check source data verification (SDV), and audit-ready trial binders.
Full-time, experienced Clinical Research Coordinators integrated directly on-site to handle trial workflows without disrupting routine patient care.
Four commitments shape every study we support, from protocol delivery to audit-ready data.
Single-point-of-contact contracting, central IRB reliance, and streamlined budget negotiations minimize cycle time from protocol delivery to first patient in (FPI).
Dedicated recruitment teams and community-based outreach ensure swift enrollment of diverse, protocol-compliant study populations.
We place experienced Clinical Research Coordinators directly into partner clinics, seamlessly integrating research procedures without disrupting standard clinical workflows.
Standardized SOPs, stringent source data verification (SDV), and continuous QA ensure accurate, audit-ready data at every milestone.
Reliable data integrity, predictable recruitment, and rapid startup metrics across diverse therapeutic areas.
Submit a Protocol / Sponsor InquiryJoin our investigator network with a full-time, experienced Clinical Research Coordinator embedded on-site, so trials run alongside routine patient care.
Partner With UsGain access to potential new medical treatments, complimentary health evaluations, and study-related care under expert medical supervision.
Become a Patient Volunteer