Descripción
Descripción: Responsbilities & Duties:
- To administer, maintain and coordinate the logistical aspects of the clinical trials according to GCP and SOPs.
- Work side-by-side with CRA and CTMs and assisting ...
Requisitos: Mandatory:
-English Advanced Level
-Advanced IT Skills
-Previous experience in a similar position as a CTA or other position such as Study Coordinator related to clinical research environment
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Tipo de contrato
Sin especificar
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Salario
No disponible