Revise detenidamente toda la documentación de la solicitud antes de hacer clic en el botón de solicitar al final de esta descripción.
(Study site selection, initiation (SIV) and clinical monitoring.
• Prepare and conduct SIV to ensure adequate study training for relevant site staff to proceed with study start and conduct in compliance with protocol and relevant regulations.
• Conduct monitoring visit according to SDV plan and SOP; address issues with sites and complete monitoring visit report in a timely manner coordinating.
• Training
• Provide ongoing training to site staff with regards to ICH-GCP, GCP, study protocol and requirements.
• Finalize budget and obtain signed contract from site, prior to site initiation visit.
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