As a Manager Pharmacovigilance you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence. You will be partnering with a pharmaceutical company committed to discovering ...
Clinical System Designer II ICON plc is a world‑leading healthcare intelligence and clinical research organization..., and we welcome you to join us on our mission to shape the future of clinical development. We are currently seeking a Clinical System Designer II to join ICON...
Magnéticos nacionales y distritales) - Preparación soportes y cumplimiento controles ICON - Calculo provisión de impuestos...
Senior Clinical Trial Manager (Senior CTM) & Clinical Trial Manager (CTM) The Senior Clinical Trial Manager and Clinical Trial Manager profile is responsible for the end-to-end operational oversight of assigned clinical trials, ensuring d...
goals, and the overall operations of the clinical research site. COMs verify that CTAs are performing to ICON standards...
Regulatory submission manager ICON is a global healthcare intelligence and clinical research organisation united.... As a General submission manager at ICON, you will contribute to drug development as part of the Regulatory Affairs team...
Desktop Publishing Specialist - Language Services - Homebased - Colombia and Brazil (Only) ICON plc is a world... Publishing Specialist in ICON Language Services provides project preparation and DTP assistance to translation project managers...
de administración y desarrollo de proyectos de la variedad de soluciones tecnológicas que ICON Management está implementando. Esta... persona realizará demostraciones y/o adiestramientos al staff de ICON, clientes internos y externos, actualizaciones...
Graduate PV - Remote - Colombia ICON plc is a world-leading healthcare intelligence and clinical research... to join our diverse and dynamic team. As a Graduate Pharmacovigilance Associate at ICON, you will play an essential role in supporting the...
ICON is seeking a Senior Clinical Trial Manager to oversee the end-to-end operational management of clinical trials...