management of clinical trial sites by assisting with site monitoring activities, ensuring compliance with study protocols... monitoring of clinical trial sites, ensuring adherence to study protocols, regulatory requirements, and Good Clinical Practice...
and monitoring of clinical trial sites by ensuring compliance with study protocols, regulatory requirements, and Good Clinical... monitoring activities at clinical trial sites, ensuring adherence to study protocols and timely resolution of site-related issues...
of clinical trial sites by ensuring compliance with study protocols, regulatory requirements, and Good Clinical Practice (GCP... activities at clinical trial sites, ensuring adherence to study protocols and timely resolution of site-related issues...
. As a Site Management Associate I at ICON, you will play an important role in supporting the management of clinical trial sites... and logistical support to site management teams. What You Will Be Doing: Assisting in the monitoring of clinical trial sites...
– a highly skilled, accomplished network that spans more than 180 sites, 24 countries and 6 Strategic Business Units (SBUs...
that spans more than 180 sites, 24 countries and 6 Strategic Business Units (SBUs). Our industry-leading experts are setting the...
and maintenance of investigative sites to ensure that sites are activated in line with the study timelines and client expectation...
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Veracruz, Ver. | 21/01/2026 18:01:01 PM | Salario: S/. No Especificado | Empresa:
ICON. As a Site Management Associate I at ICON, you will play an important role in supporting the management of clinical trial sites... and logistical support to site management teams. What You Will Be Doing: Assisting in the monitoring of clinical trial sites...
and participates in incident investigations. Technical Acumen Reviews engineering documentation/designs, sites, and building plans...
and monitoring of clinical trial sites by ensuring compliance with study protocols, regulatory requirements, and Good Clinical... monitoring activities at clinical trial sites, ensuring adherence to study protocols and timely resolution of site-related issues...