Physician Benefits
Global Health Network assists their physicians by providing them with the following value-added benefits:
Access to Quality Clinical Trials...
Access to Quality Clinical Trials…
Global is constantly in touch with CROs and industry sponsors of clinical trials. We will contact you by fax, phone or e-mail with new prospective studies that are suitable to your specialty and practice. Should you be potentially interested in the trial, we will arrange for a detailed protocol to be forwarded, once you complete a non-disclosure form. We also work closely with you to obtain local IRB approval. For investigators who do not have a local IRB, we will provide access to and coordinate communications with a central IRB.
At Global, we make quality patient enrollment a number-one priority. The success or failure of a clinical trial rests on the ability to target and recruit qualified patients to participate through the entire trial period. We will help you determine if your practice can support the enrollment target for proposed clinical trials.
Throughout the entire process, we facilitate effective coordination of information between sponsor, investigator and patient.
We encourage you to apply for inclusion among our Select Sites. All information provided to us on the investigator form will be entered into our confidential database. This will enable us to quickly identify the right trials to suit your research needs, and forward these breaking trials to your attention as they develop. We contact Select Sites first to determine your interest in a proposed trial before releasing this information to third parties. Unlike other SMOs Global is not a research broker.
Our database of investigators is national in scope and constantly growing. We currently partner with over 750 board-certified physicians in a variety of specialties. Global works with the finest physician investigators in the nation. All of our investigators are in private practice, affiliated with renowned medical teaching facilities or affiliated with public hospitals around the country. All have extensive experience working with clinical trials.
Because we work so closely with our investigators and study sponsors, our success rate for completing clinical trials is high.
Global Site Support Resources (GSSR) is a unique new service provided by Global to all of our investigators. We developed this program for investigators who are dedicated to research and who have the recruitment capabilities, but are either short-staffed or have a vacancy in their CRA department and need site support. Through this service, Global delivers efficient on-site study coordinators, utilizing well-trained (using Good Clinical Practice (GCP) Standards), highly skilled Clinical Research Associates (CRAs).
Global offers the most quality focused and cost efficient way to achieve effective study execution at the site level by supplying the site with professional, experienced CRAs who already possess the necessary technological and research knowledge.
Global negotiates a contract with the sponsor on behalf of all of our investigators participating in a particular trial. We will then help you set up a study budget, and enter into a contract with you directly to support that budget. We will monitor the budget and your success in enrolling patients, and pay you directly according to our contract.  |
|
|
|
|
|
|
|
|
|
 |
 |
 |
 |
 |
 |
|
|||
 |
|
||||||||
 |
|
|
|||||||
 |
 |
|
|||||||
 |
|
||||||||
 |
|
||||||||
 |
|
||||||||
 |
|
||||||||
 |
|
||||||||
 |
 |
|
|||||||
 |
|
||||||||
| |
|||||||||