Reaching Results
Through Research.
The Research Center of The Upstate is a premier clinical research organization dedicated to advancing medicine through innovation, integrity, and compassionate care — bringing elite clinical research options directly to the Upstate community.
Our Story & Commitment
Founded in 2017, The Research Center of the Upstate is committed to improving the quality of life through cutting-edge clinical research. We partner with sponsors, physicians, and participants to conduct high-quality clinical trials that contribute to the development of safe and effective treatments for a wide range of medical conditions.
We uphold the highest standards of scientific rigor, patient safety, ethical conduct, and regulatory compliance, ensuring every study is conducted with excellence, integrity, and respect for those who entrust us with their care.
Our Mission
To improve the quality of life through cutting-edge clinical research by upholding the highest standards of scientific excellence, patient care, and ethical conduct while delivering results that drive meaningful advancements in healthcare.
Our Vision
We aspire to honor God by using clinical research as a tool for healing, education, and innovation. Through integrity, compassion, and faithful stewardship of our resources, we strive to impact lives positively, advance medical science, and set the standard for excellence in clinical research.
Uncompromising Integrity
Strict adherence to FDA, GCP, and HIPAA guidelines ensures every data point is valid and every participant is protected.
Compassionate Care
We treat participants as partners in discovery, providing regular clinical monitoring and dedicated support throughout.
Clinical Excellence
Led by board-certified physicians and experienced clinical staff with over 17 years of medical expertise.
Our On-Site Diagnostic Services
Our modern Greenville facility is fully equipped to perform the standard and advanced diagnostic protocols required by global pharmaceutical sponsors.
Electrocardiogram (ECG)
Advanced cardiac monitoring integrated into trial protocols to ensure participant safety and capture precise cardiac data.
Nutrition & Weight Loss
Structured educational programs and trial pathways focused on sustainable metabolic health, nutrition, and lifestyle medicine.
Physical Examinations
Comprehensive physicals conducted by licensed physicians to monitor health baselines and confirm eligibility for specialized research.
Comprehensive Blood Testing
On-site blood draws and advanced hematology profiles to track metabolic markers, safety panels, and drug efficacy.
Diagnostic Lab Testing
Laboratory analysis of biomarkers and safety endpoints, processed under strict quality controls.
Serology & Viral Markers
Precise antibody testing and viral tracking to evaluate immune responses, vaccine trials, and infectious disease markers.
How Clinical Trials Work
Participating in clinical research is a structured, supportive, and entirely voluntary process. Here is what you can expect when you partner with us.
Initial Consultation
Discuss your medical history, lifestyle, and wellness goals with our clinical staff to determine your eligibility for active trials.
- Comprehensive history review
- No-cost preliminary screening
Trial Enrollment
Once eligible, begin participation with the continuous guidance of our medical team. We explain every protocol, timeline, and expectation clearly.
- Detailed protocol briefing
- Informed consent process
Ongoing Care
Receive regular clinical monitoring, diagnostic testing, and direct access to advanced medical resources — all at no cost to you.
- Continuous health monitoring
- Time & travel compensation (select trials)
Ready to take the first step?
Our clinical team is ready to guide you. Learn about active trials and see if you qualify today.
Meet Our Investigators & Staff
Our clinical trials are directed by board-certified family physicians and highly trained study coordinators who bring years of research experience and medical excellence to Greenville.
Founder and owner with 17+ years of clinical research experience. Leads the center with a focus on participant care and operational excellence.
Board-certified physician with extensive clinical trial experience. Oversees all research protocols and ensures FDA compliance.
Experienced physician specializing in clinical research. Provides medical oversight and participant care throughout each study.
Family Nurse Practitioner with 17+ years of medical expertise. Provides clinical assessments and participant support.
Certified Medical Assistant providing direct participant care and clinical support. Ensures smooth trial operations.
Manages regulatory documentation and compliance. Ensures all trials meet FDA, GCP, and HIPAA standards.
Need direct coordination? Contact Yolanda Livingston at [email protected]
Have Questions About Clinical Trials?
Clinical research can feel unfamiliar. Here are answers to the questions participants ask most.
Still have questions?
Our team is happy to talk. We can explain trial criteria, safety standards, and compensation in plain, reassuring language.
Ask Our Team DirectlyWhat is a clinical trial?
Clinical trials are carefully designed research studies that test new medical treatments, drugs, or devices in people. They are the essential path to discovering safer, more effective ways to prevent, diagnose, and treat disease.
Is there any cost to participate?
No, and no insurance is required. All study-related medical care, laboratory tests, and trial medications are provided to participants at no cost. Many trials also offer compensation for your time and travel.
How are patient safety and privacy protected?
Participant safety is our highest priority. Every trial is reviewed by an Institutional Review Board (IRB) and complies with FDA guidelines and HIPAA privacy rules. Our medical team monitors you closely throughout the study.
Can I leave a study once it has started?
Yes. Participation in clinical research is entirely voluntary. You may withdraw from a trial at any time, for any reason, without affecting your standard medical care.
We'd Love to Hear From You
Whether you are a potential participant, medical provider, or pharmaceutical sponsor, contact our Greenville office to discuss clinical collaboration.
Office Location
2086 Woodruff Rd. Suite A
Greenville, SC 29607
Phone & Fax
Office: 864-626-3117
Fax: 864-203-3888
Office & Trial Hours
Mon–Thurs: 8:30am–3:30pm
Fri–Sun: Closed
Privacy policies and intake forms are provided directly via secure email and onsite during participant visits.
Patient Stories & Feedback
We are deeply committed to professional excellence and compassionate care. See what participants from our Greenville community are saying about their experience.
Read Our Google Reviews