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