Review and interpret the data provided by the PCO to establish the system / tools required to be populated in line with current standard operating procedures or business process documentation, including systems and SOPs associated with the regulatory data scope.
Lic. QFB, QFI, Ingles avanzado INDISPENSABLE, deseable experiencia en estudios clínicos, experiencia mínimo de 3 años en Asuntos regulatorios, protocolos
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