SGM will assume the responsibility of running your trial. This allows for the best utilization of your time with the least disruption of your normal clinical day.
We will provide a trained experienced Clinical Research Coordinator to be available at your site on designated patient days. Our experienced coordinator will negotiate your contract with the pharmaceutical company to get the maximum reimbursement allowable.
The Clinical Research Coordinator will also, conduct patient visits in accordance with the Protocol and assist the Physician in the proper documentation process of GCP Guidelines. In addition, the Research Coordinator will advise the Physician of the procedures that will need to be completed according to protocol and will assist when necessary.
The Clinical Research Coordinator will also complete the Electronic Data Capture per the Pharmaceuticals requirements and all source documentations. In addition to completing the necessary documentation for the submission of Serious Adverse Event and follow-up documentation, this will allow the physician to complete minimal source documents.
The Clinical Research Coordinator will also process and ship lab samples. They will document and track all drug shipments and maintain drug accountability logs and temperature logs in accordance with the protocol guidelines.
For more information, please contact Lucinda Little, CCRC at 610-999-3437 or at firstname.lastname@example.org