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Why CNS

Diversity. 

Experience. 

Infrastructure. 

Experience.

Capabilities. 

Since 1996, we have served thousands of medical heroes and helped bring 94 drugs to market.

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Diversity

Enhancing clinical trial diversity is a moral and scientific imperative, and while diversity in clinical trial participants is a buzz these days CNS Healthcare can proudly say that since opening our doors in 1996, improving the enrollment of participants from underrepresented racial and ethnic populations in clinical trials has always been at the forefront of our conduct of research. Our sites are in diversely populated areas making our databases full of different races, ethnicities, and ages to best support the safety and efficacy of a trial.

Experience​

When clinical trial sponsors look for a partner to conduct research, experience is key. Since 1996, CNS Healthcare has worked with the most well-known and up and coming companies in the pharmaceutical industry to safely and effectively carry out trials that bring therapeutic medications to market. CNS has extensive experience in conducting trials has given us a unique perspective into the mindset of pharmaceutical companies. We understand sponsors’ expectations when conducting a trial and we are constantly striving to exceed them.

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Infrastructure

We like to think of ourselves as more than just a cookie-cutter research organization. Every research team cares about patient safety, but do they offer 24/7 availability for patients to have their questions answered? We do! We also continue delivery of care for patients after the completion of a trial and until they are prepared for the next step in their journey to wellness. Our commitment to the well-being of patients spans well beyond their physical health—we also go to great lengths to ensure their protected health information is safe. We use world-class cybersecurity platforms, have a dedicated IT department, and utilize processes developed by the FBI to avoid data breaches.

Expertise​

Successful clinical research requires a special group of people with specific and unique skill sets like those who we’ve placed on our team. We have a genuine interest in every patient that walks through our doors, and that’s reflected in the care our skilled teammates deliver. Our team of dietitians, nurses, psychiatrists, internists, endocrinologists, neurologists and family medicine physicians have the expertise needed to shape the future of medicine.

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Capabilitites

  • Medical professionals with decades of clinical and research experience
  • Board Certified, full time Principal Investigators
  • 100% Investigator oversight and involvement at every visit with documented progress notes
  • Dedicated teams of Study Coordinators who are experienced Nurses and/or Master’s level clinicians and certified raters
  • Primary and back-up Study Coordinators to manage each trial
  • Full time pre-screening clinician 
  • Full time Data Managers and Phlebotomists, in addition to teams of full-time Research Assistants
  • Involved in over 2500+ Phase 1-4 clinical trials with pediatric, adult and geriatric patients
  • Experience in decentralized and hybrid studies
  • 94 drugs to market and counting 
  • Committed patient recruitment team, including full-time community liaisons in each location 
  • Large patient database and referral network for all indications
  • Onsite and remote 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
  • Dedicated, independent clinical research centers
  • Ability to be an early start site with quick regulatory submission and 24-hour contract negotiation
  • Telemedicine Capabilities and COVID-19 SOPs
  • Multipurpose mobile research unit available to travel into the community
  • Over 10,000 sq. ft. of devoted research facilities
  • On site lab with full capabilities, IATA certifications, and CLIA waiver
  • Refrigerated and ambient centrifuges
  • IV infusion room
  • Temperature and alarm monitored drug room, sub-zero freezers, and drug refrigerators
  • Biometric (fingerprint) access to drug room
  • DEA compliant, dual-lock, bolted steel drug cabinets
  • Vertical laminar flow hood in an ISO space 
  • Fiber optic connectivity for security and data integrity
  • High speed internet access  
  • Proprietary CTMS 
  • State of the art firewalls and 24/7 infrastructure monitoring services
  • Dedicated regulatory teams 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, clean FDA and Sponsor audits for high enrollment
  • Internal Regulatory managing platform
  • 4-6 Private, individual monitoring rooms each with a 2-person capacity
  • Access to a phone, fax, copier, and high-speed internet
  • Full time EDC personnel for rapid data entry and query resolution
  • Experience with remote and risk-based monitoring systems 
  • Medical professionals with decades of clinical and research experience
  • Dedicated to conducting clinical trials 
  • 100% Investigator oversight and involvement in every visit with documented progress notes
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Therapeutic Areas
  • Addiction
  • Allergy
  • Cardiovascular
  • Dermatology
  • Device
  • Emergency Medicine
  • Endocrinology
  • Family Medicine
  • Family Practice
  • Gastroenterology
  • Healthy
  • Immunology
  • Infectious Disease Prophylaxis and Treatment
  • Internal Medicine
  • Nephrology
  • Neurology
  • Obstetrics and Gynecology (OB/GYN)
  • Ophthalmology
  • Orthopedics
  • Otolaryngology (ENT)
  • Pediatrics
  • Physical Medicine and Rehabilitation
  • Preventive Medicine
  • Psychiatry
  • Urology
  • Vaccine

Types of Trials

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Patient Populations

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Specialty and Diverse Patient Access

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Equipment, Procedures and Facilities

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Sites Capabilities

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Recruitment

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State of the Art Facilities

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Technology

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Regulatory/QA

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Monitoring

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Clinical Trial Experience

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Principal Investigators

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Coordinators / Support Team

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Research Partners

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Your Trial Opportunity