Site Monitoring Associate I (Belén de Escobar)
Site Monitoring Associate I (Belén de Escobar)
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Belén de Escobar, Argentina
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Publicado: hace menos de una semana
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Descripción
Site Management Associate I (FSP
- Sponsor dedicated) ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development. As a SMA I at ICON, you will support the management of clinical trial sites by assisting with site monitoring activities, ensuring compliance with study protocols, and maintain high standards of operational efficiency. What You Will Do: Your role will involve delivering clinical research work to a high standard, working closely with your team and stakeholders. Key responsibilities include:
- Assisting in the monitoring of clinical trial sites, ensuring adherence to study protocols, regulatory requirements, and Good Clinical Practice (GCP) guidelines.
- Supporting site management activities, including documentation preparation, data entry, and tracking site performance metrics, eTMF filing , audit preparation support
- Initiation of investigator site activities, including collection of site essential documents
- Manage supply/resupply shipments to sites, support on study country insurance requests and applicable updates
- Collaborating with cross-functional teams to facilitate communication and address site-related issues effectively.
- Maintaining accurate records of site activities and contributing to the preparation of monitoring reports.
- Participating in training and development initiatives to enhance knowledge and skills in clinical trial management.
Your Profile:
- Bachelor's degree in a relevant field such as life sciences, healthcare administration, or clinical research.
- Clinical research experience or relevant experience preferred
- Strong organizational skills and attention to detail, with the ability to manage multiple tasks effectively. Basic knowledge of clinical trial processes and regulatory requirements is a plus.
- Excellent communicatio Postúlate en Kit Empleo: kitempleo.com.ar/empleo/qalos
- Sponsor dedicated) ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development. As a SMA I at ICON, you will support the management of clinical trial sites by assisting with site monitoring activities, ensuring compliance with study protocols, and maintain high standards of operational efficiency. What You Will Do: Your role will involve delivering clinical research work to a high standard, working closely with your team and stakeholders. Key responsibilities include:
- Assisting in the monitoring of clinical trial sites, ensuring adherence to study protocols, regulatory requirements, and Good Clinical Practice (GCP) guidelines.
- Supporting site management activities, including documentation preparation, data entry, and tracking site performance metrics, eTMF filing , audit preparation support
- Initiation of investigator site activities, including collection of site essential documents
- Manage supply/resupply shipments to sites, support on study country insurance requests and applicable updates
- Collaborating with cross-functional teams to facilitate communication and address site-related issues effectively.
- Maintaining accurate records of site activities and contributing to the preparation of monitoring reports.
- Participating in training and development initiatives to enhance knowledge and skills in clinical trial management.
Your Profile:
- Bachelor's degree in a relevant field such as life sciences, healthcare administration, or clinical research.
- Clinical research experience or relevant experience preferred
- Strong organizational skills and attention to detail, with the ability to manage multiple tasks effectively. Basic knowledge of clinical trial processes and regulatory requirements is a plus.
- Excellent communicatio Postúlate en Kit Empleo: kitempleo.com.ar/empleo/qalos
Información clave
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Nombre de la empresaIcon Strategic Solutions
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Nombre de la vacanteSite Monitoring Associate I (Belén de Escobar)
Consejos de seguridad
Tené cuidado con trabajos prometedores que no exigen demasiado.
Más info sobre el aviso
El aviso Site Monitoring Associate I (Belén de Escobar) fue publicado en la categoría Escobar Informática, telecomunicación de Locanto.
En estos momentos, este es el único aviso disponible en esta categoría en Escobar.
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