Proper site management adds positive momentum to successful patient recruitment, which secures the success of clinical trial deliverables.
Our site management services contract with the trial sites (hospitals and medical institutions) and assist with complex trial work so that trials can be properly conducted per GCP guidelines without interruption.
In usual practice, site management activities depend on the capabilities CRA. But, in complex studies, We have extended our site management services through a site management organization. WE collaborates with medical institutions (hospitals and/or clinical research institutions)/ Principal Investigators to enhance the site’s performance at the site level. The benefit of this practice is that it ensures robust patient recruitment and retention. With input from both the CRA and the site’s services (via SMO), we can ensure optimal use of clinical trial time and resources.
A full range of site management organization services that are your assurance of successful clinical trials.
- Provide study coordinator to work with the site (hospital or medical institution) / Principal Investigators to support the principal investigator (PI) in ethics committee submissions, patient recruitment, and follow-up.
- Our assigned study coordinator assists the site in creating the project’s specific working documents.
- Set up the clinical trial process to meet specific project requirements.
- Suppprt the sites to achieve overall project deliverable from the sites’ perspective