Research Champions/Sponsor/CRO

Our philosphy is Pursuit for Excellence. Welcome to Clinical Inquest Center and thanks for your interest in considering us to assist you in your efforts to successfully execute clinical trials.. We understand and take very seriously your goals and are committed to do everything that we can to ensure the successful outcome of your clinical investigation. Please contact us to discuss how we may be able to work with each other.

Our mission is to provide you with efficient and experienced sites, investigators, coordinators, regulatory and quality assurance staff.. You may be managing your trial internally or utilizing the services of a Contract Research Organization, we can efficiently speed up the site identification, screening, initiation, budget/contractual negotiations and start up process. Our standard operating procedures and core management team are specifically designed to quickly provide you with multiple and highly qualified sites that meet your specific criteria.

We assign a Business Manager, Project Manager to your study to assist with early centralized communication. This increases efficiency by eimianating the time you spend answering similar site generated queries.

We share a great relationships with many quality CRO's. Our experience section under Why CIC ? will impart enough confidence in you to select as your number one SMO now and always.. Additionally, as the CRO may have previously worked with a particular site, they are familiar with its capabilities and past performance. This can significantly reduce time and resources expended during the site identification and qualification process. Having an established relationship between the monitor and site can also reduce monitoring time and expense.

Pursuit for Excellence in Quality

All of the Investigators in the CIC-AMERICA network are highly experienced clinicians and researchers. We are not a clinical research training ground! In order to become a part of our network, a physician must demonstrate that they have successfully participated in 3-5 clinical studies.

Clinical Research Coordinators must also meet stringent criteria. Since we place an enormous amount of responsibility for the success of your study on them, we ensure that they have the skills and capabilities to manage it appropriately.

Productivity and Controls

We have a comprehensive database of investigators amd is very easy for us to identify investigators based on your specific needs, a significant amount of your time and resources are saved during the initial site identification, screening, and qualification of our investigators.

We are just a phone call away and that will assist you in selecting numerous investigative sites. You are always free to select only those sites that you want to use. .

Budgetary and contractual discussions are always centralized, thus minimizing lengthy negotiations for each site. Upon agreement of a budget (which is applicable across all sites), a clinical trial agreement can typically be executed within one week or less.

CIC-AMERICA, Company Highlights

• Provide multiple, quality sites
• Ability to conduct Phase I through Phase IV studies
• Large database of highly skilled and experienced Investigators
• Dedicated, full time, and experienced Clinical Research Coordinators
• Currently we provide coverage in Ohio, but are expanding at a rapid pace and will be adding more locations soon
• Access to large patient populations
• Centralized contract and budget resolution
• Ability to conduct inpatient and outpatient studies
• Strong working relationships with local and central IRB's and laboratories
• Established and stable relationships with large public, private and military institutions
• Track record of consistently meeting or exceeding enrollment goals
• Aggressive patient recruitment program
• Expertise to conduct even the most challenging studies
• Effective and mutually beneficial working relationships with Investigative sites

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