Site Management (SMO)
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Qualified study coordinators and site management associates are key to the successful management of a clinical trial.
Novotech’s 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.
Novotech’s SMO services are currently only available for clinical trials taking place in South Korea and Taiwan.
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|