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Answers to common questions from patients, sponsors, and physicians about clinical research at Solutions Research Group.
Our team is happy to help. Reach out and we will respond within 1 to 2 business days.
A clinical trial is a research study that tests how well a new medication, treatment, or approach works and how safe it is for people. Every approved treatment available today was first studied in a clinical trial with volunteers.
Each study has its own eligibility criteria, such as age, health history, and current medications. Some studies look for people with a specific condition, while others need healthy volunteers. Our pre-screening form helps us understand which studies may be a good fit for you.
We are preparing for upcoming studies. Complete the pre-screening form and our team will contact you when a study matches your profile, so you are among the first to hear about new opportunities.
No. Study-related exams, lab tests, consultations, and investigational treatments are provided at no cost to you, and medical insurance is not required.
Qualified participants often receive compensation for their time and travel. The amount depends on the study and its visit schedule, and it is always explained to you before you decide to join.
No referral is needed. You can apply directly through our pre-screening form. You are also welcome to keep seeing your own doctor while you take part in a study.
Our Patient Recruitment Specialist reviews your answers within 1 to 2 business days. If your profile matches a study, a Clinical Coordinator will call you to explain the details, compensation, and next steps, and to schedule a screening visit if you are interested.
Yes. Taking part in a clinical trial is always voluntary, and you can choose to leave a study at any time for any reason.
Study visits take place at our research site at 6300 W 159th St Suite A, Oak Forest, IL 60452.
Every study is reviewed and monitored by an independent Institutional Review Board (IRB) whose role is to protect participant rights and safety. All visits, health evaluations, and procedures are handled by licensed healthcare professionals, and you are monitored closely throughout the study.
Before you join any study, our team explains its goals, procedures, schedule, and potential risks and benefits in clear language. You can ask as many questions as you like, and you only join after you fully understand the study and sign the consent form.
Yes. Your information is strictly confidential and is used only to evaluate your eligibility and coordinate your participation. It will never be sold or shared with third-party advertisers.
We operate as a dedicated clinical trial site, providing study startup, participant recruitment and retention, protocol execution under qualified Principal Investigators, and clean, audit-ready data from kickoff to closeout.
Our startup process is built for speed, with a 24 to 48 hour regulatory turnaround target, central IRB reliance, and streamlined budget and contract negotiation to reduce the time to First Patient In.
We use practical community outreach to enroll suitable participant groups, supported by dedicated Clinical Research Coordinators, visit reminders, and proactive engagement to work toward a 90%+ retention standard.
Our workflows follow ICH-GCP guidelines and FDA standards, supported by standardized SOPs, source data verification (SDV), continuous quality assurance, and audit-ready trial binders.
Use the Sponsor Inquiry form on our Sponsors & CROs page and our team will follow up on site feasibility, timelines, and next steps.
Yes. We work with physicians and practices interested in bringing clinical research to their patients, with our team handling the operational and regulatory workload.
We place experienced Clinical Research Coordinators directly into partner clinics, so research procedures are integrated into the practice without disrupting standard patient care.
Send us a message through our Contact page and select Physician / Investigator Inquiry, or call us at 708.289.3032.
Talk to our team directly, or start your pre-screening application and a coordinator will be in touch.
