ICON plc is a world-leading healthcare intelligence and clinical research organization. We're proud to foster an inclusive environment driving innovation and
.As a Senior Clinical Site Manager you will be joining the world's largest & most comprehensive clinical research organisation, powered by healthcare
Pfizer Clinical Study Team Lead (Director) in Bothell , United States JOB SUMMARY . • Clinical Development expert focused on the execution of clinical
Clinical Quality Compliance Lead job in Madrid | ICON __vacancyopjusttionswidget.opt-Business Area__ ICON Strategic Solutions
JOIN US ON OUR EXCITING JOURNEY! IQVIA is The Human Data Science Company, focused on using data and science to help healthcare clients find better solutions
Job OverviewUnder moderate supervision, executes the feasibility, site identification regulatory, start-up, and maintenance activities in accordance with
Position Summary:The Senior Clinical Data Manager is responsible and manages all aspects of the clinical trial data management process from study start up to
EmailPosition Summary:The Senior Clinical Data Manager is responsible and manages all aspects of the clinical trial data management process from study start up
.At ICON, it's our people that set us apart. Our diverse teams enable us to become a better partner to our customers and help us to fulfil our mission to
col-wideJob Description:Oncology patients are waiting for personalized cancer care options. What if your Senior Clinical Project Manager expertise was the only
.At ICON, it's our people that set us apart. Our diverse teams enable us to become a better partner to our customers and help us to fulfil our mission to
At ICON, it's our people that set us apart. Our diverse teams enable us to become a better partner to our customers and help us to fulfil our mission to
Prepares and / or reviews regulatory documents to support clinical trial submissions. Independently provides regulatory support for more complex
Prepares and / or reviews regulatory documents to support clinical trial submissions. Independently provides regulatory support for more complex
EmailPosition Summary:The Senior Clinical Data Manager is responsible and manages all aspects of the clinical trial data management process from study start up
Position Summary:The Senior Clinical Data Manager is responsible and manages all aspects of the clinical trial data management process from study start up to
Join Caidya as a Senior Study Start-Up Lead (Sr. SSUL). You'll focus on managing the submission of global applications for clinical trials. The ideal candidate
.Position Summary:The Senior Clinical Data Manager is responsible and manages all aspects of the clinical trial data management process from study start up to
.EmailPosition Summary:The Senior Clinical Data Manager is responsible and manages all aspects of the clinical trial data management process from study start
.- Budapest, Dublin, Warsaw, Lisbon, Johannesburg, Barcelona, ReadingICON plc is a world-leading healthcare intelligence and clinical research organization.