With so many options to choose from, why do top pharmaceutical companies from around the world choose CNRI to conduct their clinical trials time and again?
 
Experienced Staff: CNRI’s professional, experienced leadership team will make the clinical trial process as seamless as possible from beginning to end. Many of our investigators have worked on over 100 clinical trials over the past ten years at CNRI. Dr. Tran-Johnson has over 25 years of research experience in the Academic setting and as Director of Research/Principal Investigator at CNRI for over 250 CNS trials. Our Sr. Project Manager, Robert Perkovic, also has 20 years of research experience at CNRI. CNRI’s expertise in clinical trials is recognized by CROs and sponsors via repeat business.
 
Clinical Excellence: CNRI meets or exceeds sponsor and CRO recruitment quotas in over 95% of our studies. CNRI also has high subject retention rates consistent with the study design and the ratio of drug-placebo for any given study. Our use of customized source documents and internal auditing insure quality control of each study. CNRI is well known for producing data that demonstrates excellent result separation between active drug and placebo. Our doctorate level raters for psychiatric studies have over 15 years of rating experience and high inter-rater reliability. As a result, our Principal Investigator is frequently asked to be first or second author of professional journal articles as well as Signatory Investigator for FDA submissions.

 

On-Site Clinical Research Unit: all inpatient studies (Phase I - IV, PSG/Sleep, Healthy Volunteer) are conducted at the Clinical Research Unit located in the same building.
 
Efficiency: CNRI’s large database and referral network of both stable and acute relapse patients mean that we can recruit appropriate subjects quickly for Phase I-IV studies. Our physicians review labs and ECG results daily. We also enter data rapidly, and respond to queries promptly. One of our goals is to do our best to help sponsors adhere to the planned time line for a given study.
 
Convenient Locations: CNRI’s clinics are based centrally in both the San Diego and the Los Angeles area, giving us access to the highest numbers of patients and allowing us to select only the most appropriate subjects for each study. Our accessible locations and on-site transportation significantly improves patient retention in studies.
 
Quality Patient Care: One of our goals is to ensure a safe, pleasant and informative experience for our patients. We treat research subjects with compassion and respect. 
  
These are just some of the reasons that the majority of our trials has been re-awarded from the same sponsors and CROs. Our extensive list of sponsors and professional references are a testament to the quality of services we provide.