Welcome to River City Clinical Research


Clinical trials move medicine forward. Sponsors, such as pharmaceutical companies, governments and foundations fund medical research. Patients who participate in clinical research receive many advantages including treatment at no cost, access to expertise and resources such as expensive tests. Research volunteers shape the future and can have fun while helping others and themselves.

 

As a premier clinical research organization, we have conducted more than 2,500 clinical trials over 20 years and have worldwide recognition for providing patients access to cutting edge medical research. If you have a medical issue and want a research solution, or if you are a healthy volunteer, come visit our center and learn more. One of our experts will be happy to evaluate you.


Shape the Future

Clinical research is a process that gives back. Volunteers generate information that improves future health care outcomes for everyone.

Find relief with new treatments

Volunteers join research to seek relief from affliction and to better understand their conditions with support from our caring team.

Programs Offer Resources or Pay

Study participants receive medical tests, services, counseling and treatment at no charge. These measures may be unavailable to the general public!


We do research in many areas


Herniated Disc


ENROLLING SOON!

If you have a Herniated Disc, you may qualify for one of our studies.

Qualified volunteers may receive at no cost:
  • investigational medication
  • study-related care from a local doctor
  • possible compensation
Health insurance isn’t required to participate.
Ask your doctor or contact our clinic for more information
(904) 861-3050
Or sign up below!

Anemia Due To Chronic Kidney Disease


How is anemia related to chronic kidney disease?

Anemia commonly occurs in people with chronic kidney disease (CKD)—the permanent, partial loss of kidney function. Anemia might begin to develop in the early stages of CKD, when someone has 20 to 50 percent of normal kidney function. Anemia tends to worsen as CKD progresses. Most people who have total loss of kidney function, or kidney failure, have anemia.1 A person has kidney failure when he or she needs a kidney transplant or dialysis in order to live. The two forms of dialysis include hemodialysis and peritoneal dialysis. Hemodialysis uses a machine to circulate a person’s blood through a filter outside the body. Peritoneal dialysis uses the lining of the abdomen to filter blood inside the body.

We have a clinical trial enrolling now for patients with anemia due to chronic kidney disease. If you want to learn more call (904) 861-3050
or sign up below!


**If this study doesn't work for you, check out our other STUDIES **





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Our Volunteers Love Us


Watch what they have to say about their research experience!



Postpartum Depression Research Testimonial
Phase 1 Research Joe's Experience
Phase I Research Terry's Experience

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Our Staff

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Emery Noles

Emery Noles is the Site Manager at River City Clinical Research and has been with ENCORE Research Group since 2002.  She loves to spend time with her husband, her two children and golden retriever; especially while at the beach. During her trips to the beach, she loves to look for shark’s teeth to add to her collection, “once I get started looking for shark’s teeth, I can’t stop…it’s addicting!” Emery also collects wine corks, and for bottles on special occasions, she will write the event and date on the cork. 

Some of Emery’s other favorite things involve: reading, gardening and running. She also loves to watch Modern Family “I can relate to Claire on all accounts!”. When it comes to sports, her favorite teams are East Carolina Pirates and the Florida Gators. During the games you might find one of Emery’s favorite foods pizza or tacos on her dinner table, which are also foods the whole family loves!  

Shannon Schultenover

Shannon Schultenover works at the River City Clinical Research branch of Encore Research Group.  She has been with the Encore Research community for one and a half years now and is currently a Coordinator in Training and phlebotomist.

Shannon loves to spend time with her son. Together they enjoy arts and crafts and playing superheroes. Shannon also loves to run and play her favorite sport, soccer.  Speaking of sports, Shannon is an avid Chicago fan. She loves all of the Chicago teams and cheers for the Bears, Cubs, Blackhawks and Fire.

Shannon may be an expert on superheroes and villains, but now it’s time to start buffing up on her Disney princesses. She and her husband are expecting their second child this coming January 2017 and IT’S A GIRL!

 

Lastest Blog Post:


Clinical Trial Insight

Thank You for a Great Year!

As an ENCORE community member, we hope you have enjoyed hearing from us this year. Each month we strive to provide you with accurate information on health topics that are relevant to you and our enrolling studies. 2018 has been a momentous year for us and has seen complete many trials for novel medications that we believe will improve global health. We are thankful for dedicated volunteers like you that make this possible!

This month we would like to do something a little different and provide you with insight into clinical trials. A lack of clinical trial education is routinely cited as the number one barrier to enrolling trial participants. Clinical trials are required by the FDA to prove the safety and effectiveness of new medications and volunteer participants are necessary to complete these trials. We understand that this concept is often intimidating. However, there are several measures in place to make our trials as safe as possible, including:
•Physicians in charge of all study activities
•Pre-Clinical Testing
•Institutional Review Boards (IRBs)
•Informed Consent Forms
•Routine Participant Labs and Clinical Assessments
•Clinical Trial Data Safety Monitoring Boards

Investigational products are thoroughly studied during pre-clinical testing before the trials are designed and the first human participant is enrolled. Pharmaceutical companies spend millions of dollars to bring medications to market and they want to be nearly certain that the medication will fulfill its intended purpose. However, volunteers are needed to complete the FDA clinical trials. When designing the trial protocols, participant safety is always the number one priority!

Every trial is overseen by an Institutional Review Board (IRB). The purpose of the IRB is to protect the rights and welfare of human research participants. The IRB evaluates the possible risks and benefits of the trial before it is allowed to open. They are also responsible for approving the trial protocol and the informed consent. Along with the consent form, a discussion with our medical staff allows you to make an informed decision on whether or not the trial is in your best interest. Lastly, participants in the study are continuously monitored for safety and there are many tests completed during the trials to alert researchers at the first sign of potentially serious side effects. We hope that every patient that has worked with us has felt that it has been a safe and positive experience!

Thank you again for helping us improve global health and find new ways to treat medical ailments! 2019 is going to be another exciting year at ENCORE Research and we hope to get the chance to work with everyone reading this letter. 

Happy Holidays,
ENCORE Research
 

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