Who We Are
Independently Owned - Clinical Research Team

• We are a private and independently owned and operated alliance of dedicated research centers.

• We foster open, honest and frequent communication so that the inevitable unforeseen challenges, common to every clinical trial, are identified and managed before becoming serious threats to the study outcome.

• We are a team of clinical research professionals that have conducted over 370 clinical trials in a broad range of therapeutic areas, including, but not limited to, cardiology, CNS, dermatology, endocrinology, infectious disease, device, oncology and rheumatology.

• We have a diverse environment and patient pools that play a major role in the success of patient recruitment and retention at our three locations. New investigators continue to call on us to become a part of our diverse therapeutic area.

• We also have a network of consulting professionals we contract with to work in protocol development and report writing. Because of our extensive experience and access to MCR Inc's group of consultants, we can tailor our CRO/SMO services to our clients needs.

What We Do
Dedicated Clinical Research Center - Expert Team - Knowledgeable

• We are a dedicated clinical research center and pride ourselves in quality research.

• We have dedicated in-house principal investigators and also an ever-growing network of community-based physicians to conduct Phase II - IV clinical trials.

• We have an expert team of professionals for the recruitment and screening of patients to ensure our sites are prepared for every phase of recruitment. Our success is based upon reaching and retaining patients quickly and efficiently. We achieve this by researching the needs of the patient, knowing the different characteristics that individual patients bring to a clinical trial, their motivation to participate, and issues that can impact recruitment.

• We provide teams of highly qualified and experienced clinical research professionals to conduct all aspects of clinical trials.

• We have the knowledge, experience and resources for generating accurate source documentation, case report forms and staff to complete case report forms promptly, to meet the needs of your project.

• We will evaluate each clinical protocol for feasibility, ensuring that we will only take on a trial we know that we can provide the required number of subjects within the specified timelines.

• We are willing to work with any central or local IRB that you choose.

• We are able to work in the latest electronic data capture system that you require.

Benefits Using MCR Inc.
Here are some of the other benefits you will find at MCR Inc.:

• Rapid enrollment rates
• Easy access to investigators
• Metropolitan population exceeding three million
• Large population of university students
• Two fully equipped state of the art Facilities
• Investigator/Sub Investigators and certified research coordinator staff dedicated solely to clinical research
• Computerized database with over 3,300 previous patients
• On staff full-time Patient Recruiters
• A full time quality assurance Director
• A dedicated staff for data entry, EDC or paper CRF transcription

What We Believe
Integrity - Accuracy - Promptness

• We conduct every trial with attention to quality and integrity.

• We pride ourselves on accuracy and promptness.