The role of the Clinical Research Associate (CRA) is pivotal in any clinical research project. SOCAR's experienced and fully trained CRAs ensure that the clinical research studies are conducted in accordance to ICH GCP and specific ISO guidelines (as appropriate) in addition to the study protocol. In between the regular site visits, our CRAs are in close contact with the research sites either by email or telephone, thus enabling early identification of problems and ensuring their prompt resolution.

SOCAR provides the following clinical study monitoring services:

Site selection visits
Initiation visits
Site monitoring visits
Close-out visits

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