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                                          Clinical Research

Where Research is the Answer

Since 1996, CNS Healthcare has served thousands of medical heroes like you. Learn more about research with us; schedule a free consultation today.

Memphis, TN

6401 Poplar Avenue, Suite 420
Memphis, TN 38119
Phone (901) 843-1045 ▪ Fax (901) 843-1206
Main contact:
Kelly Iskiwitz - Site Administrator



  • Dedicated, independent research center
  • Serving over 2 million people in the Greater Memphis, Tennessee area; Arkansas and Mississippi
  • Experience in most therapeutic indications
  • Phases 1, 2, 3, and 4
  • Pediatric to Geriatric patients
  • Serial ECGs and Serial PK sampling
  • Ability to be an early start site with quick regulatory submission and 24 hour contract negotiation


  • Committed patient recruitment team including a full time community liaison
  • Large database and referral network for all indications
  • Face to face pre-screen assessments
  • Ability to track our return on advertising campaigns
  • Mass texting and emailing for appointment reminders and notification of upcoming studies
  • Patient verification system to prevent enrollment of professional patients
  • Strategic alliance with local, medical multi-specialty groups


  • Over 7,000 sq. ft. devoted to research
  • On site lab with CLIA waiver
  • Refrigerated and ambient centrifuges
  • IV infusion room
  • Temperature and alarm monitored drug room, subzero freezers, and drug refrigerators
  • Biometric (fingerprint) access to drug room
  • DEA compliant, dual-lock, bolted steel drug cabinets


  • Fiber optic connectivity for security and data integrity
  • Use of your own VPN on our dedicated high speed internet access for monitors and visitors
  • Proprietary trial management software used for scheduling and tracking patient visits
  • State of the art firewalls and 24/7 infrastructure monitoring services 


  • Dedicated regulatory specialist with prompt document turnaround time and strong working relationship with all Central IRBs
  • Strong QA program with dedicated QA specialist and use of internal SOPs
  • Numerous successful FDA and Sponsor audits for high enrollment


  • 4 individual monitoring rooms, each with a 2 person capacity
  • Access to a phone, fax, copier, and high-speed internet


  • Involved in over 350 clinical trials
  • 70 drugs to market and counting
  • Indications include: Addictions, ADHD, Alzheimer’s disease, Anxiety Disorders, Autism, Auto Immune Disorders, Cardiovascular Disorders, Dermatology, Diabetes, Diabetic Peripheral Neuropathy, Down Syndrome, Eating Disorders, Gastrointestinal Disorders, Influenza, Men’s Health, Migraine, Mood Disorders, Obesity, Pain, Respiratory, Schizophrenia, Sleep Disorders, Smoking Cessation, Vaccines, Women’s Health


  • Over 120 years combined research and clinical trial practice; each with 20 to 40 years of experience
  • 100% Investigator oversight; involvement in every visit with documented progress notes
  • High inter-rater reliability across medical assessments (diagnostically and across symptom rating scales) and continuous training


  • 6 Study Coordinators each with 3 to 20 years of experience
  • All Study Coordinators are experienced Nurses and/or Master’s level clinicians and certified raters on most scales
  • Primary and back-up Study Coordinators dedicated to each trial
  • Full time RN pre-screener
  • Full time Data Manager and Phlebotomist, in addition to two full-time Research Assistants


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