Our Solutions
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Our Solutions
Clinical Research Alliance has a lot to offer, whether you are a Physician interested in expanding your catalogue of Clinical Trials without having to manage or finance the research infrastructure, or if you are a patient seeking highly experienced and qualified physicians who can offer our trials.
Clinical Research Alliance has a lot to offer, whether you are a Physician interested in expanding your catalogue of Clinical Trials without having to manage or finance the research infrastructure, or if you are a patient seeking highly experienced and qualified physicians who can offer our trials.
Clinical Research Alliance has a lot to offer, whether you are a Physician interested in expanding your catalogue of Clinical Trials without having to manage or finance the research infrastructure, or if you are a patient seeking highly experienced and qualified physicians who can offer our trials.
Select on any of the buttons below to learn more.
These coordinators are on site for study visits. The CRA team is in communication with the sub-site every step of the way to ensure that only eligible patients are enrolled, and there is a strict adherence to protocol. CRA offers this service to dedicated and knowledgeable physicians who understand the importance of clinical research but lack the infrastructure to perform clinical trials independently. This has become an obstacle for many physicians across the nation.
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CRA offers to community physicians a research team of qualified study coordinators with years of experience in the field.
Due to current trying economic times and an inability to provide necessary funds to keep a research program afloat, many physicians’ offices have disbanded their research department. In an effort to solve this issue for physicians, CRA provides its members with the advantage of having mobile study coordinators in their office without the expense of maintaining their salaries, equipment, etc.
For Physicians
CRA offers to community physicians a research team of qualified study coordinators with years of experience in the field.
For Physicians
These coordinators are on site for study visits. The CRA team is in communication with the sub-site every step of the way to ensure that only eligible patients are enrolled, and there is a strict adherence to protocol. CRA offers this service to dedicated and knowledgeable physicians who understand the importance of clinical research but lack the infrastructure to perform clinical trials independently. This has become an obstacle for many physicians across the nation.
Due to current trying economic times and an inability to provide necessary funds to keep a research program afloat, many physicians’ offices have disbanded their research department. In an effort to solve this issue for physicians, CRA provides its members with the advantage of having mobile study coordinators in their office without the expense of maintaining their salaries, equipment, etc.
Clinical Trial Planning
We collaborate with you to develop efficient and informative
clinical development plans.
On trial, these patients enjoy the benefit of being closely monitored—not only by their physician, but also, by our research team, who are on site at all study visits. In addition to the high quality of care they are already receiving, they have the added attention and expertise of a devoted research team, which further enhances their quality of care. These study coordinators operate directly under the physician at the sub-site within the framework of the protocol.
Regulatory Management
In addition to clinical oversight, CRA has facilitated research at sub-sites by establishing centralized regulatory management and contractual services.
This centralization expedites the research process, so that sub-sites need not worry about the ‘nitty-gritty’ of conducting clinical trials, such as submission to an IRB, negotiation of the contract, sending out regulatory documents for study start-up, maintaining a study file, and other clinical requirements.
Ready to Get Started?
For Patients
Clinical Trial Planning
Clinical Research Alliance gives the patients in our physicians’ offices, some with life-threatening disease, an opportunity to enroll on a clinical trial employing new, innovative treatment therapies.
For Patients
Clinical Research Alliance gives the patients in our physicians’ offices, some with life-threatening disease, an opportunity to enroll on a clinical trial employing new, innovative treatment therapies.
On trial, these patients enjoy the benefit of being closely monitored—not only by their physician, but also, by our research team, who are on site at all study visits. In addition to the high quality of care they are already receiving, they have the added attention and expertise of a devoted research team, which further enhances their quality of care. These study coordinators operate directly under the physician at the sub-site within the framework of the protocol.
Ready to Get Started?
For Hospitals
In addition to clinical oversight, CRA has facilitated research at sub-sites by establishing centralized regulatory management and contractual services.
This centralization expedites the research process, so that sub-sites need not worry about the ‘nitty-gritty’ of conducting clinical trials, such as submission to an IRB, negotiation of the contract, sending out regulatory documents for study start-up, maintaining a study file, and other clinical requirements.
Our capable research team handles all these aspects. Without having to concern themselves with these, sometimes tedious, facets of clinical research, physicians and clinical personnel can focus solely on patient care and still have the opportunity to enroll their patients on clinical trials.
Click on the icons below to learn more
For Physicians
CRA offers to community physicians a research team of qualified study coordinators with years of experience in the field.
These coordinators are on site for study visits. The CRA team is in communication with the sub-site every step of the way to ensure that only eligible patients are enrolled, and there is a strict adherence to protocol. CRA offers this service to dedicated and knowledgeable physicians who understand the importance of clinical research but lack the infrastructure to perform clinical trials independently. This has become an obstacle for many physicians across the nation.
.jpg)
Due to current trying economic times and an inability to provide necessary funds to keep a research program afloat, many physicians’ offices have disbanded their research department. In an effort to solve this issue for physicians, CRA provides its members with the advantage of having mobile study coordinators in their office without the expense of maintaining their salaries, equipment, etc.
For Patients
Clinical Research Alliance gives the patients in our physicians' offices, some with life-threatening disease, an opportunity to enroll on a clinical trial employing new, innovative treatment therapies.
On trial, these patients enjoy the benefit of being closely monitored—not only by their physician, but also, by our research team, who are on site at all study visits. In addition to the high quality of care they are already receiving, they have the added attention and expertise of a devoted research team, which further enhances their quality of care. These study coordinators operate directly under the physician at the sub-site within the framework of the protocol.
For Hospitals
CRA is committed to providing hospitals with turnkey clinical trial research solutions, allowing their patients access to life-saving drugs and therapies.
This centralization expedites the research process, so that sub-sites need not worry about the ‘nitty-gritty’ of conducting clinical trials, such as submission to an IRB, negotiation of the contract, sending out regulatory documents for study start-up, maintaining a study file, and other clinical requirements.
Without having to concern themselves with these, sometimes tedious, facets of clinical research, physicians and clinical personnel can focus solely on patient care and still have the opportunity to enroll
their patients on clinical trials.
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