About Clinical Research Center of Alabama
Clinical Research Center of Alabama has been conducting clinical research studies since 1998. Our center has conducted hundreds of clinical studies in adult and pediatric patients, and has contributed to the development of new therapies for asthma, allergic rhinitis, eczema, hives, other skin conditions, hereditary angioedema (HAE), chronic obstructive pulmonary disease (COPD). The Clinical Research Center of Alabama conducts Phase II, III, and IV clinical trials for both large and small pharmaceutical companies and Contract Research Organizations. Our research center has earned a reputation for excellence. Our physician investigators are Board Certified in Internal Medicine and Pediatrics and in Asthma, Allergy and Immunology. Dr. Weily Soong and Dr. John Anderson are on the teaching faculty at the University of Alabama School of Medicine (UAB) and have published multiple research articles. All of our physician investigators have been certified in clinical research. Our dedicated clinical research staff is highly trained and experienced. Our center has six certified clinical research coordinators (CCRC). All coordinators and investigators have completed the CITI training program from the University of Miami, and our research staff includes a nurse practitioner, a registered nurse, a registered respiratory therapist and other well trained professionals.
Clinical Research Experience
The Clinical Research Center of Alabama conducts Phase II, III, and IV clinical trials for both large and small pharmaceutical companies and Contract Research Organizations. Our research center has earned a reputation for excellence. Our center reaches and exceeds the expected recruitment and randomization goals with qualified compliant study patients. Due to rigorous and careful screening, our center has enjoyed high completion rates with minimal numbers of screen failures. We accurately document all study procedures, tests and events, maintaining complete and accurate source documents and timely completion of case report forms. The Clinical Research Center of Alabama is able to work with centralized Institutional Review Boards.
Weily Soong, MD
John Anderson, MD
Maxcie Sikora, MD
Sunena Argo, MD
Carolyn Comer, MD
William Massey, MD
Lorena Wilson, MD, MHS
Patricia Luthin, CRNP
Blake Youngblood, CRNP
Michelle Payne, CRNP
Annie Ketcham, CRNP
Erin Cuzzort, CRNP
Monica Ray, CRNP
Becca Watkins, CRNP
Stephanie Edwards, CRNP
J. Christopher Davis, MD, FACS
Amanda Denham, MD
Michael Sillers, MD
Kelli Phillipson, RN
Clinical Trials Revenue Specialist
Beth Hagerty, CCRC
Diane Paige, CCRC
Kendra Williams, LPN, CCRC
Kaylee Hale, CCRC
Kellie Steager, CCRC
Carla Honeycutt, CCRC
Trey CaJacob, CCRC
What is a clinical research study?
- A research study involving human volunteers is conducted to answer specific health questions.
- Carefully conducted clinical research studies are the safest and fastest way to find treatments that work in people and new ways to improve health.
- Research studies are conducted according to a plan called a protocol.
- A protocol describes what types of patients may enter the study; schedules of tests and procedures, drugs, dosages, and length of study, as well as outcomes that will be measured.
- Each person participating in the study must agree to follow the protocol.
Why are research studies conducted?
- To see if a new drug or device is safe and effective for people to use.
- To compare existing treatments to determine which is better.
- To study different ways to use standard (approved) treatments, so they will be more effective, easier to use, and/or decrease side effects.
- To learn how to best use the treatment in a different population, such as children, in whom the treatment was not previously tested.
How are participants protected?
- To protect the rights and welfare of clinical research participants, U.S. Federal Agencies including the Food and Drug Administration (FDA) & the National Institutes of Health (NIH) oversee much of the medical research in the U.S.
- Institutional Review Boards (IRBs) oversee the centers where clinical research studies are conducted.
- IRBs review and approve study protocols to ensure that a clinical trial is ethical and that volunteers’ rights are protected.
- A participant in a clinical trial has access to the IRB that is overseeing the research and access to a volunteer advocate, the physician and staff conducting the trial.
- Federal agencies inspect individuals and institutions conducting research. They also inspect IRBs.
- Some IRBs are accredited much like hospitals can be “accredited” and some research investigators and staff are “certified” as research professionals.
What are some of the possible benefits of my participation?
- Gain access to potentially new research treatments.
- Receive expert medical care for the condition being studied, since investigators are often specialists in the disease area being studied.
- Help others by contributing to medical research and treatment advances.
- Receive financial reimbursement for time and travel.
What are some of the possible risks of my participation?
- There may be unpleasant, serious, or even life-threatening side effects resulting from the treatment.
- The treatment may not be effective.
- Participation in the trial may be demanding and time consuming.
Affiliations & Accolades
Join Our Team
The following positions are currently open:
CLINICAL RESEARCH COORDINATOR – view a description of the position and apply HERE.