Site Management (SMO)
Qualified study coordinators and site management associates are key to the successful management of a clinical trial.
CLINISYD Site Management (SMO) service provides highly qualified and experienced Study Coordinators (SCs) and Site Management Associates (SMAs) to help support both principal investigators and sponsors. Through our SMO service, we provide principal investigators with trained SCs to assist with daily clinical trial activity and patient Recruitment and sponsors with experienced SMAs to provide clinical trial site management and ethics committee support.
SITE MANAGEMENT SERVICES INCLUDE:
Program Development & Start-up
| Program Development & Start-up Study management | Ethics Committee communication and management |
| Site contract, budget, expense management | GCP documents / training review |
| Subject recruitment and retention management | Quality Control |
| Subject safety management | Third party Vendor management |
| Ensuring Study compliance | Logistics management |