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A dedicated clinical research site in Oak Forest, Illinois, partnering with pharmaceutical sponsors, CROs, and local participants to run studies built on patient safety and accurate data.
At Solutions Research Group, we connect medical research with practical community care.
Operating as a dedicated clinical trial site, we partner with pharmaceutical sponsors, CROs, and local participants to run clinical studies focused on patient safety and accurate trial data.
Our role is simple: give sponsors a site they can rely on, and give participants an experience that is clear, respectful, and well cared for from the first call to the final visit.
Dependable protocol execution, fast site activation, and audit-ready data for your next study.
Clear information, qualified medical staff, and study-related care at no cost to you.
GCP, ICH, and FDA aligned processes with independent IRB oversight on every study.
We offer the operational structure and regulatory oversight needed to keep clinical trials running on schedule while maintaining strict data integrity.
Full adherence to GCP, ICH guidelines, and FDA standards, ensuring clean, audit-ready data from protocol kickoff to study closeout.
Efficient startup processes to handle IRB submissions, budget contracts, and site preparation without unnecessary delay.
Practical community outreach strategies designed to enroll suitable participant groups and maintain strong retention rates.
Managed on-site by qualified Principal Investigators and research coordinators focused on protocol compliance and subject safety.
Medical progress relies on individuals who choose to participate in clinical trials. We treat every participant with respect and make sure you have complete clarity about what a study involves before you join.
All trial visits, health evaluations, and procedures are handled directly by licensed healthcare professionals.
We explain study goals, potential risks, expected schedules, and procedures in clear language so you can make an informed decision.
Study-related exams, consultations, and investigational treatments are provided at no cost to you. Compensation for your time and travel is typically included.
Every study undergoes review and continuous oversight by an independent Institutional Review Board (IRB) to safeguard participant rights.
Quality is built into how we work, not checked at the end. Our processes are designed so sponsors receive accurate, audit-ready data and participants stay protected throughout.
ICH-GCP compliant workflows at every stage of the study.
Site operations aligned with FDA requirements and SOPs.
Central IRB reliance with continuous review of each protocol.
Double-checked source data for accurate, clean reporting.
Standardized SOPs guide every study task, from consent to data entry.
Audit-ready trial binders maintained throughout the life of each study.
Continuous quality assurance to catch issues early and keep data accurate.
Dedicated coordinators supporting participants to reduce missed visits and dropouts.
Whether you are planning your next study or thinking about taking part in one, our team is ready to help.
Share your protocol and our team will follow up with site feasibility, startup timelines, and next steps.
Complete a short pre-screening form and a coordinator will contact you if you qualify for an upcoming study.
Have another question? Contact our team or call 708.289.3032.
