Wellstar Research Institute
Advancing patient-centered research that transforms care
Wellstar Research Institute partners with patients, clinicians and academic and industry collaborators
to deliver rigorous clinical research that improves health outcomes across diverse communities.
- Wellstar Research Institute
- About Us
- Our Partnerships
- Our Supporters
- For Participants
- Research Oversight
About Us
A Mission for Innovation
At the Wellstar Research Institute, we are committed to advancing innovative, patient-centered research that improves health outcomes and shapes the future of care. Our current areas of focus reflect the most pressing health needs of our communities, with dedicated research in:
- Cardiovascular Health
- Oncology
- Neurosciences
- Trauma
Academic Partnerships
Strategic Collaborations Driving Innovation
Our academic partnerships enhance the scope, quality and translational impact of our research. These relationships support shared goals in biomedical discovery, health equity, education and workforce development.Premiere Research Partners
Augusta University
As a strategic academic partner, Augusta University produces a range of collaborative research initiatives with Wellstar. Augusta University executes over 400 clinical trials at Wellstar MCG Health Medical Center previously known as Augusta Hospital and Medical Center.Kennesaw State University (KSU)
WRI and KSU are primed to collaborate on interdisciplinary research and innovation, including joint projects in public health, data analytics, nursing, and community-based interventions. Our partnership strengthens academic-practice integration, and fosters opportunities for faculty and student engagement in clinical research.Georgia State University (GSU)
Through our partnership with GSU, we have opportunities to focus on public health, epidemiology, and social determinants of health. The collaboration has paved the way for joint efforts in grant funded research, health equity and health literacy initiatives, and a range of other nursing focused areas of shared interest.Mercer University
We have expanded our longstanding clinical partnership with Mercer University to include academic practice research, laying the groundwork for future joint research initiatives.Advancing Knowledge Through Collaboration
Through these strategic academic alliances, WRI is building a robust, multidisciplinary research ecosystem that fuels discovery, improves patient outcomes, and prepares future leaders in healthcare. Interested in exploring academic collaborations?Submit a Collaboration Inquiry Form
Sponsors & Industry Partnerships
Capabilities & services
- Full-service study start-up and site activation
- Regulatory and IRB coordination
- Recruitment, enrollment and retention strategies tailored to diverse populations
- Data management, monitoring and high-quality source documentation
- Post-marketing and real-world evidence studies
Why partner with WRI
- Proven enrollment performance
- Broad geographic reach within Wellstar Health System
- Robust regulatory and compliance oversight
- Commitment to ethical, patient-centered research
For Participants
What to know about clinical research?
The Basics | National Institutes of Health (NIH)Participating in clinical research
Participating in Human Research and Clinical Trials | HHS.govWhat to Expect When Participating in Clinical Research
If your doctor thinks you may be a good fit for a research study, they may talk with you about the opportunity to participate. Joining a clinical study is always your choice, and our goal is to make sure you have all the information you need to feel comfortable and confident about your decision.Talking with Your Doctor
Your doctor may refer you to a clinical study if it’s related to your condition or care. They’ll explain why the study might be a good option for you and connect you with our research team for more information.Meeting the Research Team
Once referred, you’ll meet with a research nurse or study coordinator—a member of our team who will guide you through every step of the process. They’ll answer your questions, schedule your study visits, and make sure you understand what will happen at each visit. You’ll see this same team regularly throughout the study.Informed Consent
Before you decide whether to join a study, you’ll review and sign a document called informed consent. This is not just paperwork—it’s a conversation. The research team will explain:- The purpose of the study
- What procedures or tests are involved
- How long the study lasts
- Any possible risks or benefits
- Your rights as a participant, including the option to stop at any time
During the Study
Throughout your participation, you’ll work closely with the research team at each visit. They’ll monitor your health, collect information, and keep your doctor updated on your progress.Costs and Billing
Some of the care you receive during the study—such as doctor visits, lab tests, or medications you would have gotten anyway—are part of standard medical care and may be billed to your insurance. Other activities that are only for research purposes—like special study tests or extra visits—will be paid for by the study sponsor, not you.Our team will review this information with you in detail before you decide to join, so there are no surprises about costs or billing.
Institutional Review Board
Who should submit
Residents, fellows, medical students, investigator-initiated trials and collaborative research partnersSubmission materials
- IRB initial submission application
- Study protocol (link to template)
- Informed consent form (link to template)
- HIPAA authorization or waiver requests
- Recruitment materials and CVs