Job Description
Experteer Overview
¿Listo para inscribirse? Antes de hacerlo, asegúrese de leer todos los detalles pertenecientes a este trabajo en la descripción a continuación.
In this role you support clinical study activities for a sponsor as part of the SRS/FSP team at a global CRO. You drive accurate data entry, timely issue resolution, and quality study support to keep milestones on track. You’ll assist with regulatory submissions, investigator interactions, and patient recruitment, contributing to efficient trial conduct. This position offers growth in a collaborative, values‑driven environment that improves patient outcomes. You will work across monitoring visits, ethics processes, and study logistics to enable successful trials.
Compensaciones / Beneficios
• Data entry and query resolution
• Assist SAE notification
• Support investigator with patient recruitment
• Facilitate Ethics Committee submissions
• Attend Monitoring Visits, Audits and Inspections as needed
...
¿Listo para inscribirse? Antes de hacerlo, asegúrese de leer todos los detalles pertenecientes a este trabajo en la descripción a continuación.
In this role you support clinical study activities for a sponsor as part of the SRS/FSP team at a global CRO. You drive accurate data entry, timely issue resolution, and quality study support to keep milestones on track. You’ll assist with regulatory submissions, investigator interactions, and patient recruitment, contributing to efficient trial conduct. This position offers growth in a collaborative, values‑driven environment that improves patient outcomes. You will work across monitoring visits, ethics processes, and study logistics to enable successful trials.
Compensaciones / Beneficios
• Data entry and query resolution
• Assist SAE notification
• Support investigator with patient recruitment
• Facilitate Ethics Committee submissions
• Attend Monitoring Visits, Audits and Inspections as needed
...
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