Your Local Research Partner

M3 Wake Research Chattanooga stands as a prominent clinical research facility within the M3 Wake Research network, dedicated to enhancing healthcare through rigorous clinical trials across a variety of medical fields. 

With over 56 years of combined experience across a wide range of therapeutic areas and specialties, M3 Wake Research Chattanooga offers opportunities to participate in clinical trials that support advancing care. Explore current studies to learn more and see if you may qualify.

If you are interested in a specialty or study not currently listed, complete our general survey to stay up-to-date with current and upcoming studies.

Meet the Team

Our principal investigators at M3 Wake Research Chattanooga are board-certified in their areas of specialty and highly experienced in clinical research. With our experienced principal investigators leading every clinical trial we support at our Chattanooga research site, we are dedicated to ensuring not only the integrity of every clinical trial, but also the collection of data to sufficiently study the medical device, treatment or therapy being tested. Meet our principal investigators who’ll be conducting the clinical trials at M3 Wake Research Chattanooga. 

Principal Investigator 

Family Medicine

Board-certified family medicine physician with 9 years of clinical research experience. Dr. Ballard is known for her collaborative approach and deep connection to the Chattanooga medical community.

Principal Investigator 

Neurology, Neurophysiology

Taylor Bear, MD is a board-certified neurologist and academician with 20+ years of experience as a physician and 5+ years of clinical research experience. He has also completed his Fellowship in Clinical Neurophysiology. 

Principal Investigator 

Internal Medicine

Board-certified internist and hospitalist with 5+ years of multi-therapeutic clinical research experience.

Sub-Investigator

Family Medicine

Board-certified neurologist and academician with 5+ years of
clinical research experience. He has completed his Fellowship in Clinical Neurophysiology. 

Meet principal investigator example.
Meet the team example.

Our team at M3 Wake Research Chattanooga is highly experienced in supporting sponsors and CROs with conducting a wide variety of clinical trials. As a leader in the clinical research industry, M3 Wake Research understands that importance of clinical trials for the advancement of medical science and improving patient outcomes for years to come, and we take pride in ensuring the safety and comfort of our participants. We work diligently throughout the entire clinical research process, helping to recruit patients according to the trial protocol, scheduling clinical visits, and following up between visits in case of any emergencies. Meet our clinical research team to learn who you’ll be interacting with during throughout the clinical trial. 

Site Manager 

Erica is a certified clinical research coordinator (CCRC) by ACRP since 2013. She brings more than 20 years of clinical research experience to M3 Wake Research Chattanooga. Erica has worked at M3 Wake Research Chattanooga for nearly 12 years across all phases of trials for a variety of indications. 

What is Clinical Research?

Clinical research is a vital component of medical advancement, involving human subjects to test new treatments, medications, or medical devices. This type of research is essential for developing new medical interventions, as it allows researchers to gather preliminary data on the safety and effectiveness of these treatments. Conducted in our Chattanooga clinical site, clinical research is led by our dedicated research team. By participating in clinical research, human subjects contribute to the crucial process of medical discovery and innovation. 

Benefits of Participating in Clinical Studies 

Participating in clinical studies offers numerous benefits, including access to cutting-edge treatments that may not be available through standard care. These studies play a pivotal role in advancing medical knowledge, leading to improved treatments and better patient outcomes. Participants have the unique opportunity to work closely with a research team, contributing to the development of new therapies. Moreover, clinical studies are meticulously monitored by healthcare professionals to ensure participant safety, and strict regulations and guidelines are in place to protect participants throughout the study. 

Ensuring Participant Safety 

Ensuring the safety of participants is a top priority in clinical research. Institutional review boards (IRBs) rigorously review and approve clinical studies to ensure they meet stringent safety and ethical standards. Throughout the study, our team closely monitors participants to mitigate any risks. Informed consent is a critical component, ensuring that participants are fully aware of the potential risks and benefits before joining a clinical study. Additionally, clinical studies are designed to minimize risks, and participants have the right to withdraw from the study at any time, ensuring their safety and autonomy.