Clinical Start-Up

Position SummaryThe Clinical Start-Up & Trial Lead (Start-Up + CTL) is responsible for the strategic planning, coordination, and oversight of clinical trial start-up activities as well as the ongoing execution of clinical studies. This hybrid role ensures operational excellence from site initiation through to study close-out, serving as the primary...

Clinical Start-Up & Trial Lead – FortreaThe Clinical Start-Up & Trial Lead (Start‑Up + CTL) is responsible for the strategic planning, coordination, and oversight of clinical trial start‑up activities as well as the ongoing execution of clinical studies. This hybrid role ensures operational excellence from site initiation through to study close‑out,...

Clinical Start-Up & Trial Lead – Fortrea The Clinical Start-Up & Trial Lead (Start‑Up + CTL) is responsible for the strategic planning, coordination, and oversight of clinical trial start‑up activities as well as the ongoing execution of clinical studies. This hybrid role ensures operational excellence from site initiation through to study close‑out,...

Overview Join to apply for the Clinical Start-Up & Trial Lead role at Fortrea . The Clinical Start-Up & Trial Lead (Start-Up + CTL) is responsible for the strategic planning, coordination, and oversight of clinical trial start-up activities as well as the ongoing execution of clinical studies. This hybrid role ensures operational excellence from site...

Sr Clinical Site Navigator (Senior Start-up Specialist) Join to apply for the Sr Clinical Site Navigator (Senior Start-up Specialist) role at Fortrea . Job Overview The Clinical Site Navigator role is a hybrid position that combines start-up and iHCRA/CRA responsibilities. Site Navigators play a critical role in coordinating site-level activities throughout...

The Clinical Site Navigator role is a hybrid position that combines start-up and iHCRA/CRA responsibilities. Site Navigators play a critical role in the comprehensive coordination of site-level activities throughout the start-up phase of a clinical trial and potentially through closeout activities as required. Serving as the single point of contact for...

OverviewOur LATAM clinical trial activities are growing rapidly, and we are currently seeking a full-time, office-based Regulatory Submissions Manager to join our Study Start Up team in Sao Paulo! This position plays a key role in the study start up process at Medpace. ResponsibilitiesEfficiently manage and successfully execute all aspects of global...

Overview Our LATAM clinical trial activities are growing rapidly, and we are currently seeking a full-time, office-based Regulatory Submissions Manager to join our Study Start Up team in Sao Paulo! This position plays a key role in the study start up process at Medpace. Responsibilities Efficiently manage and successfully execute all aspects of global...

OverviewOur LATAM clinical trial activities are growing rapidly, and we are currently seeking a full-time, office-based Regulatory Submissions Manager to join our Study Start Up team in Sao Paulo! This position plays a key role in the study start up process at Medpace. If you want an exciting career where you use your previous expertise and can develop and...

Study Start Up Associate II - Hybrid - Brazil 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 We are currently seeking a Study Start Up Associate...