LIVING OUR MISSION AND VALUES
It is what makes us an exceptional organization. Each of us plays an important role in bringing your innovation to life. At CMRA Research center we work together to provide a comprehensive range of services. Our common purpose is to advance clinical research through speed, quality and reliability.
OUR FOCUS IS CLINICAL RESEARCH
It is always a race to do more with the time we have, to bring innovation to market sooner and to enhance more lives. These ends are best achieved by CMRA Research team because our primary mission is recruiting participants faster, executing more consistently and providing the highest quality data in the industry, every day.
WHAT MAKES US UNIQUE?
It is the way we align skill, speed and competency to create advantages for you. Our experienced investigators are among the best in the world. We back them with a professional staff, company-wide standards, central management and the unity of our wholly-owned centers. It is how we weave these elements and bind them to a common purpose with your research goals that makes the difference.
LEADERS IN CLINICAL RESEARCH
CMRA Research medical doctors are premier scientists. Our medical doctors have completed an average of 105 clinical trials and have 25 years of clinical research experience. They are thought leaders who are published in leading journals and are frequent speakers. As leaders in their specialized fields, their insights move clinical research to a higher level.
TALENTED PEOPLE, WELL PREPARED
We staff our center with the top talent needed to efficiently and effectively assess, recruit, start, conduct and complete your clinical study plans. We train our people continually in quality control and have an unparalleled quality assurance program to make sure the job is done right. Locally, our recruitment specialists, regulatory specialists, clinical research coordinators, nurses, lab technicians and data specialists provide the resources needed to complete your study. We are driven by a common purpose and passion to focus on your study, every day. Training never stops at CMRA Research center. Our continuous training programs keep us current with the industry and on the leading edge of scientific and medical technology allowing us to maintain focus on the care and safety of our participants. With hundreds of sponsors, thousands of studies and hundreds of thousands of study participants we have created a vast wealth of knowledge. Our know-how and focus keeps us on the leading edge of advanced clinical conduct.
YOUR TRIAL GOALS ARE OUR #1 PRIORITY
OVER 3000 POTENTIAL PARTICIPANTS in our database. This dynamic resource helps us match your study criteria to our assets in the most comprehensive way. We have vast experience recruiting participants. We know that the most vital recruitment activities occur before the study is awarded to a center. We use our proprietary database, outreach programs and physician referral build greater success and speed. Overall, CMRA Research has delivered a 100 percent enrollment rate in contracted studies, placing us in the elite of clinical research enterprises. CMRA Research center has a consistent approach to recruitment using print, radio and TV advertisement in combination with a number of outreach programs with local community. We have an in-house design IRB approved materials for quick turnaround on ad creation and placement.
CMRA quality control begins with the approved Site Data Quality Plan. It includes regular, systematic evaluation of data collection, regulatory documents, monitor feedback and equipment maintenance, as well as observation and verification of clinical and laboratory skills. We create our own training materials and source documents aligned with CFRs, ICH and GCP guidelines, ensuring that all levels of CMRA staff understand compliance with the regulations. Training does not end with a new employee’s orientation, but is an ongoing monthly program giving us the leading edge in knowledge and expertise.
CMRA includes regulatory team on site. This team ensures 72 Hour turnaround time of Regulatory Documents. Documents are submitted to either Sponsor or CRO or Central IRB, according to Sponsor or CRO preference.
Our center is designed and built as specialized clinical research facility. The architectural layouts make it efficient to conduct studies and are welcoming environments for participants. We set aside areas for study monitors to be comfortable and to use our facilities as an extension of your resources.
THE BIG ADVANTAGE
When you put it all together, CMRA Research center outshine the rest. Our company can identify large numbers of study participants, organize its staff for large enrollments, maintain the highest quality standards and deliver data faster.
With one contract and one point of contact, you can conveniently line up the CMRA Research resources you need. Our CMRA Clinical Performance Manager will assess feasibility, facilitate recruitment, drive performance and oversee all aspects of your project, from study start-up to database lock.
AT YOUR SERVICE
Our system streamlines the process of securing and administering a clinical research partnership. Every step of the way you can expect outstanding communication about the status of your project. No other research organization provides this level of service.