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With more than 25 years of experience in industry and academic research, NICR participates in the development of innovative and life-saving therapies through its dedication and focus to clinical research. NICR combines the use of latest technologies, streamlined clinical operations, and extensive access to a diverse population to deliver the highest quality clinical trials for life-changing therapies.

Diverse Population
Data driven access to any disease
Diverse Southern California Population
Rare-disease reach
Large network of physician affiliation
Access to top dialysis providers

State of the Art Phase 1 Lab
Dedicated Phase 1 Lab
State of the art capabilities
PK, PD & Toxicology profile specialized

Physician Owned and Operated
30 years of experience
Academic and industry research
Dedicated Medical Advisory Review Committee

Clinical Trial Management Expertise
Over 1000 trials successfully completed
Integration of speed of research with rigorous quality standards
Flexibility to conduct any study design
Highly knowledgeable team
Extensively connected to the medical community

Full CTMS Pipeline
Centralized operation from all sites
Data management
Oversight of quality


Demographic Data

  • Start year clinical research1996
  • Phases of clinical studiesPhase I, Phase II, Phase III
  • Types of studiesDrugs, Medical Devices, Vaccines
  • PopulationsChild 2-10 yrs, Adolescent 11-17 yrs, Adult 18-64 yrs, Senior 65 yrs and over
  • Type of sitePart of a practice
  • # of employees involved in research40
  • # of investigators20
  • Number of studies last year34
  • Days openMonday, Tuesday, Wednesday, Thursday, Friday, Saturday, Sunday
  • Extended office hoursYes
  • Overnight facilitiesYes
  • Dry iceYes
  • Blinded pharmacistYes
  • Dedicated monitoring spaceYes
  • Internet access for the monitorYes
  • Onsite laboratoryYes
  • Central laboratoryYes
  • Infusion capabilityYes
  • Shipping optionsFedEx, UPS, DHL
  • Contact for regulatory documentsRyan Dudley
  • Regulatory phone number323-725-0657
  • # of days to turn around regulatory documents5 business days
  • Type of IRB used by this siteCentral
  • Appropriate storage facilities for productYes
  • Able to appropriately store Schedule II drugsYes
  • # days to turn around budget and contract7 business days