CRO Services


As a full service contract research organization, WCCT Global has performed over 200 Phase I studies and more than 360 Phase II-IV trials across a very diverse client base, since its founding in 1998. We pride ourselves in the way we execute clinical research management and handle your data at our Early and Late Phase CRO (contract research organization).  We are happy to discuss all of our CRO services and answer any questions you might have.

WCCT owns two Clinical Pharmacology Units (CPUs): a Phase I Unit in Cypress, CA and a Special Populations Unit in Costa Mesa, CA. Both units are located within two large metropolitan areas, strategically situated to recruit from a very diverse ethnic population of over 13 million people (Los Angeles County – 9.3MM, Orange County – 2.7MM, and Riverside/San Bernardino Counties – 3.1MM). There are also several major universities and community colleges nearby for recruitment of normal healthy volunteers. With over 50,000 sq/ft of research space, 180 beds (if required), and a staff of ~200 qualified employees, our Los Angeles CRO is capable of addressing demand for a high volume of patients and data in a very short period of time.

WCCT Global has a longstanding successful history of rapid enrollment of volunteers into complicated, specialized trials as well as simple, bioequivalence/bioavailability studies. As an Early and Late Phase CRO, we are always striving to exceed our Sponsors’ expectations and we have been conducting clinical research since 1998.  Suffice to say, we believe that with over 14 years of experience, we are uniquely poised to address our Sponsor’s needs across the clinical research landscape of protocol and data.

To date, our contract research organization has completed over 2,200 trials in the past 30 years.  Our team carries a balanced study perspective, with experiences at the site, CRO, Pharmaceutical, and Data Management levels.  Many team members have worked as Study Coordinators before becoming Clinical Research Associates (CRAs), and still others have worked for Data Management companies before joining WCCT in a Project Management capacity.  This cross-functional experience provides value to our Sponsors.  Additionally, WCCT owns and operates two CPUs, giving us a unique study perspective because we understand the challenges that Phase I sites endure.  WCCT has a well-trained staff of clinical research coordinators who have successfully finished an intensive 10-week GCP focused training program.  We are a full service CRO that understands research from a site, data management and patient/volunteer point of view. We are a Contract Research Organization for Clinical Data Management, Clinical Research & Clinical Trial Management in the Los Angeles – Orange County area.

Our clinical research facility provides individualized services, which can be requested on a stand alone basis or as part of an integrated “full-service” solution.

  • Product development consulting
  • Pharmacokinetic Data Analysis (TK, PK, PK/PD)
  • Regulatory affairs strategy / submission
  • Protocol design
  • Medical Writing
  • Subject Recruitment
  • Quality Control/Assurance
  • Clinical studies including:
    • Food effect studies
    • Dosage Regimen assessments
    • QTc studies
    • First in man, SAD/MAD dose escalation, PK/PD
    • Multiple dose studies
    • Drug interaction studies
    • Bioavailability, bioequivilence
    • Phase I patient studies
    • Special population studies
    • Proof of concept studies
Phase IIa- IV Development services include:
  • Clinical Operations
  • Medical and Safety Services
  • Data Management
  • Biostatistics
  • Clinical Development Support
  • Scientific & Medical Communications
Our key Early and Late Phase CRO services include:
  • Project Management of Development Programs
  • Clinical Trial Management
  • Site Management
  • Clinical Trial Monitoring
  • Patient Recruitment
  • Contract Management and Investigator Reimbursement
  • Clinical Data Management

The WCCT Global Anti-Infective/Anti-Viral/Vaccine Therapeutic Center of Excellence is comprised of a network of therapeutic experts who can provide the specialized knowledge required to address the unique challenges of developing anti-infectives.

Our contract research organization can provide guidance support for:

  • Diagnoses and treatment of infectious diseases
  • Currently available anti-infective drugs; their mode of action, efficacy and safety
  • Specific risks of anti-infective drug development and how to manage them
  • Specialized knowledge of clinical trial methodology and efficacy assessment methods
  • Relationships with key opinion leaders
  • Access to a well-established global network of investigators in infectious diseases, vaccines and public health

Our investigator data includes hundreds of anti-infective and vaccine investigative sites.