Welcome to Fleming Island Center for 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


Statin Intolerance

Statin Intolerance Research Study


For more information call:

(904) 621-0390
email: cbuda@encoredocs.com 

 

Insomnia

Insomnia Research Study


 
For more information call:
(904) 621-0390
email: cbuda@encoredocs.com 





View all active studies

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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Cindy Buda

"I do my part by managing the Fleming Island Office of Encore Research." On a daily basis I work as a Research Nurse Manager of our Fleming Island site supporting the Physician Investigators and staff in conducting clinical trials being carried out in our office. I am an original "Cheese Head" born in Green Bay Wisconsin and transplanted to Central Florida at the age of 10. I moved to Jacksonville for college and made Jacksonville my home. My greatest accomplishment is my four children. I enjoy family, cycling, travel and fishing.

Karen Schuran

“I LOVE to shop!  I would shop all the time if I could!” says Karen Schuran, who earns her shopping money by being the Research Assistant and Lab Processor at Fleming Island Center for Clinical Research. Karen has been a member of our research family for 10 years and continues to be a valuable asset to the company.
She and her husband are celebrating their 25th Anniversary of marriage this month. They have two children, a daughter and a son. Karen is also “Grandma” to a cute, fuzzy bunny named Snoopy.
Karen’s favorite sport is football, which she has been learning more about so she can keep up with the men in the house. She also likes to watch game shows like Wheel of Fortune and Jeopardy, but Karen admits her real guilty pleasure is horror movies. “I absolutely LOVE horror movies, the scarier the better!”

William Davila, MD

Dr. William Davila is the Medical Director and Principal Investigator at ENCORE Research Group’s Fleming Island Center for Clinical Research.

Dr. Davila received his Doctor of Medicine degree from Ponce School of Medicine, Puerto Rico after completing his undergraduate degree from the University of Puerto Rico. Serving in the United States Navy until 2008, he completed his internship at William Beaumont Army Medical Center in El Paso, Texas and his residency at the Naval Medical Center in Portsmouth, Virginia.

Dr. Davila is board certified by the American Board of Internal Medicine and is licensed by the state of Florida. He has been a primary care physician at Gatien and Associates since 2008. He is fluent in English and Spanish.

Fun Facts about Dr. Davila:

Hobbies:               RC Cars

Favorite Food:    Pizza

Favorite Sport:   Basketball

Favorite Movie: Gladiator

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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