Welcome to California Center for Clinical Research. Our duty to our sponsor is to conduct clinical trials with precision, reliability, and integrity. This is achieved by our unique system of accurate data collection and rapid query resolution, while maintaining the safety and rights of our study participants. We strictly adhere to our internal SOP, GCP, study-specific protocols, and IRB Guidelines.

Our sponsors can be assured that the reputation, prestige, and expertise of our institution enhance the credibility and publicity of their trial results. Close adherence to study protocol and timelines is paramount.

Investigator Expertise

Our investigators have extensive clinical research experience. View our Investigator’s CV in PDF format:

Our Study Staff

CCCR staff includes skilled clinical research coordinators; registered nurses; certified phlebotomists; patient recruiters, and psychometric raters.

Regulatory Affairs

Our center facilitates immediate turn-around times for regulatory document submissions.

Please note: Our standard overhead cost for California Center for Clinical Research is 30%.

Quality Control

Study-specific worksheets are generated and carefully designed according to the protocol, enhancing QA data and minimizing queries. Our Quality Assurance Department reviews data on a regular basis.

Recruitment Resources

We have an extensive adult database.