
Sponsors & CRO's
Partner With MCB Clinical Research Centers
At MCB Clinical Research Centers, we understand that every study depends on quality data, responsive communication, and reliable execution. Our experienced team is committed to accelerating study start-up, enrolling qualified participants, resolving queries promptly, and delivering exceptional service throughout every phase of your clinical trial.
Capabilities
Experienced Research Team
• Experienced Principal Investigator and GCP-, IATA-, and CPR-certified research staff
• Dedicated regulatory, recruitment, and clinical operations teams
• Central IRB experience across multiple therapeutic areas
• Participant-focused recruitment and retention strategies
• Rapid study start-up and efficient study execution
Facilities & Infrastructure
• Seven private examination and consultation rooms
• Large treatment and observation room
• Dedicated research pharmacy
• Four private monitoring offices with secure internet and phone access
• Restricted-access laboratory and specimen processing areas
• 24-hour Temperature-controlled investigational product storage
• 24-hour medical coverage available
• 24-hour monitored facility security and video surveillance
Laboratory & Technology
• Temperature-monitored -70°C and -20°C laboratory freezer
• Refrigerated centrifuges
• Experience with multiple electronic data capture (EDC) platforms
• Reliable High Speed Internet
Sponsor & CRO Support
• Dedicated CRA communication line with direct access to the study team during business hours
• Prompt query resolution and responsive communication
• Flexible monitoring visit accommodations
• Collaborative, solution-focused approach to study management
Why Sponsors & CROs Choose MCB
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✓ Responsive, accessible study team
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✓ Dedicated CRA phone line for direct monitor support
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✓ High-quality, audit-ready documentation
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✓ Rapid query resolution and proactive communication
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✓ Strong participant recruitment and retention
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✓ Modern research infrastructure and secure facilities
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✓ Experienced team committed to quality, compliance, and successful study execution
At MCB Clinical Research Centers, we believe exceptional clinical research begins with exceptional relationships.










Trusted by Leading Sponsors and CRO's
For over 15 years, MCB Clinical Research Centers has earned the trust of leading sponsors, biotechnology companies, and CROs by delivering high-quality clinical research and exceptional participant care.









Testimonials
“I can't say enough good things about my experience at MCBCRC. From day one, the entire team made me feel welcome, comfortable, and genuinely cared for. I was a little nervous about participating in a research study, but they took the time to explain everything clearly and made sure I always felt supported. What really stood out to me was how kind and attentive everyone was. They weren’t just going through the motions—they truly cared about my well-being and made sure I was informed every step of the way. Whether it was a simple check-in or a more in-depth appointment, I always felt like I was in good hands. Being part of this study was such a positive experience, and I’m grateful to have played a small role in the important work they’re doing. If anyone is considering joining a clinical trial, I wholeheartedly recommend MCBCRC—they are simply amazing!” -J Rutherfod
"Thank you to the whole team for being such fun to see every Friday!” -CE
"Their team is responsive, collaborative, and committed to quality. The dedicated CRA phone line makes communication seamless, and queries are addressed promptly. MCB is one of the easiest sites I've worked with." -CRA
"MCB Research is a highly organized and knowledgeable clinical research site with extremely dedicated research professionals. Their investigators are quick to respond to Sponsor requests. This is a high enrolling site and they do not compromise the quality of their data collection and documentation, and they consistently have low data entry error rates. I have had the pleasure of working with them for the past year and they are very experienced and dedicated study coordinator with a highly developed capacity for protocol understanding, study execution and they consistently maintain regulatory compliance. I would be honored to work with this site in the future due to their superior quality, high ethical standards and ability to meet study timelines."
- Senior CRA"Monitoring at MCB Clinical Research Centers has been a pleasure. The site staff is well versed in the protocol and are all experienced research personnel. They are responsive to issues and requests and seem to always meet their enrollment goals."
- Anonymous Site Manager
"I find MCB Research to be professionals committed to conducting sound research. They follow site SOPS, protocol and procedures. MCB Research team members work diligently to complete their roles in a timely fashion as well as working with the CRO team in a collaborative manner. They have also been a leading enroller in each study for which I was/am assigned. The site staff with whom I interact have always been proactive, responsive and resolution oriented.
"Dr. Andrew Sedillo has served as Principal Investigator for the projects on which I have worked. He meets with me regularly when I am on site and is available via telephone as needed outside of the IMV setting. On the rare occasion scheduling has prevented a face to face meeting during a site visit, Dr. Sedillo has phoned me to discuss visit findings. The management of MCB is onsite and checks in on both study progress and the performance of their staff."
- Anonymous Clinical Research Associate
"From a CRA perspective, the crew at MCB are great to work with. Their professionalism shows through from the beautiful entryway to the offices provided for Monitors to the individual and attentive care given by the whole team. The extensive Clinical Research experience from the top down is undeniable. All team members strive to provide impeccable data while producing quality recruitment results. There is no question they will take a challenge and run with it."
- CRA II
