Welcome!
Thank you for your interest in Charlottesville Medical Research. Our intention is to enthusiastically provide you with rapid enrollment while maintaining a strict dedication to quality control. We consistently meet our allocated subject goals in a timely manner and are frequently asked to continue enrolling beyond the initially contracted agreement.
Our physicians each maintain their own private practice. It is well documented that subjects enroll in studies if it is recommended by their physician. In addition we maintain our own database of volunteers who have previously been recruited for studies. The resulting benefit for the sponsor with which we work is that we provide non-transitory, quality subject populations from a variety of demographic and socio-economic backgrounds to enroll in clinical studies. A dedicated patient recruiter and years of experience means that we also have the marketing skills to reach out to the community for volunteers to participate in the clinical research process.

CMR demonstrates our strong commitment to quality research through SOP and protocol adherence, compliance to the International Conference of Harmonization Good Clinical Practices (ICH-GCPs), and compliance to the United States Administrative Law (Code of Federal Regulations or CFR) governing the Food and Drug Administration (FDA), an agency of the United States Department of Health and Human Services.

We firmly believe that as a valued part of your team we can successfully complete your clinical investigation to bring new medications and treatments to the marketplace. Please give us a call so that we can discuss in detail how we may be able to work together.

"I’ve worked with CMR on 2 studies recently and for each, the study coordinators, investigators and support staff have been great to work with. Polly, Penny, Evonne, and Rhonda always made themselves available to handle requests/corrections during monitoring visits, routine contacts and data locks. Drs. David and Klecan were accessible and knowledgeable about the research project and their patients in studies. The site consistently completed regulatory documents quickly, was ready to go on day 1 and for both studies was among the highest enrollers. This teamwork and professionalism CMR displays is outstanding and they’ve been a pleasure to work with. "

"As a CRA assigned to Charlottesville Medical Research, I feel privileged and honored to work with staff having superb clinical research experience, an outstanding commitment to patient safety, and an intense enthusiasm to aim high in enrollment for all of their studies, while following protocol and GCP guidelines. The staff are well organized and continue to do their best to exceed goals set by the sponsor and the administration within Charlottesville Medical Research. If and when problems do occur, the staff are immediate in their response, and together as a team they create ways to ensure that the same problem does not occur again. I look forward to working with Charlottesville Medical Research for the duration of these protocols and I hope that I will have the opportunity to work with this group many more times in the very near future."

"I just wanted to take a few minutes to share with you what a pleasure it is to work with your site. Kathy, Emily, Evonne, Tiffany, Dr. David, Dr. Pambianco and everyone else that I've worked with have been fantastic! In the 10 + years I've been monitoring, I've never come across such a wonderful site. Your site personnel are very organized, well prepared, meet or exceed enrollment with quality patients, the data is excellent, timelines are always met and everyone is very pleasant and personable as well. I will continue to send new protocols to you for review for all future studies. Thank you again for all your hard work and dedication to our studies, it is truly appreciated!"

"I have thoroughly enjoyed working with the staff at Charlottesville Medical Research. Their clinical research experience and commitment to patient safety are outstanding. It's nice to work with a responsive center that has put together all the parts to complete successful clinical trials. I hope I can work with them again soon."

"I recently had the opportunity to work with Charlottesville Medical Research (CMR) for over one year on a complex study involving subjects that had frequent visits that required them to be seen at multiple sites by two physician investigators. This was a real organizational challenge for the study team but they came through with fast recruitment, high enrollment, minimal dropouts and minimal protocol deviations. Source documentation was complete and they exhibited expertise in completing electronic case report forms as well as the use of special photography equipment required for the study. They were always ready for my monitoring visits and responded professionally to all my requests and directions. Every sponsor and CRA should have the opportunity to work with this group as they presented me with one of the easiest assignments that I have had in my research career of 20+ years."

"My company had the fortune of being the sponsor for a study run by Charlottesville Medical Research (CMR). Each and everyone at this facility could not have been more accommodating and receptive to the trainings and teachings which were required for this intensive clinical trial. As the monitor for the study, I had the extra added benefit to have worked closely with Ms. Evonne Hancock as the assigned primary site coordinator for this study. I cannot begin to elaborate on her upbeat personality, her perseverance to ensure that all data was completed with accuracy and integrity, her incredibly contagious pleasant disposition, and her consistent focus on the patients and their personal needs. Each of these positive qualities made for an extremely productive, positive, and pleasant experience and we do look forward to working with Evonne Hancock and CMR in the future."

"As a CRA with almost daily monitoring experience at Charlottesville Medical Research during 2007, I whole-heartedly recommend this site. The atmosphere is welcoming and the staff are knowledgeable, professional, conscientious, enthusiastic and well-prepared for visits. Management is readily available and supportive of the needs of staff and monitors, providing adequate space and resources along with high-speed internet access. We met our goal of 200 subjects, thanks to the positive attitude and cooperative spirit of the entire staff at CMR."

"Overall, I have found the site staff to be very experienced, organized, available and friendly. In addition, their subject recruitment & retention, and quality of data, has been very good. It has been a pleasure to work with the site staff at CMR."