Qualified study coordinators and site management associates are key to the successful management of a clinical trial

 

SATA Clinical Research 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.

 

SATA SMO services are currently only available for clinical trials taking place in South Africa

 

Site Management services include:

- Study management

- IRB management

- Site contract,

- Budget,

- Expense management

- GCP documents / training review

- Subject recruitment and retention management

- Quality Control

- Subject safety management

- Third party QC

- Ensuring Study compliance

- Logistics management