Do you have experience in creating data transfer agreements, data mapping? Are you looking to work with Electronic Health Records and be involved in a new exciting role?  

As a Risk Based Study Manager/Monitor you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.

As a Clinbical Study Lead you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.

As a Clinical Study Lead you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.

As a Clinical Research Associate you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.

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 Clinical Risk Manager.     

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 Clinical Risk Manager.     

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 Clinical Risk Manager.     

As a Senior Contract Analyst you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.

As a Senior Clinical Research Associate you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.

ICON is looking for a SSU CTA to support one of our FSP clients!! 

As a Clinical Research Associate you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.

As a Clinical Research Associate you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.

This position is accountable for the User Acceptance Testing (UAT) process for IRT systems. Through UAT, you will be key to the clinical trial process by are ensuring quality and proper functionality in a highly critical system. While following an established process, you’ll also be expected to make suggestions and deploy new ways of working that create efficiencies while maintaining effectiveness.  We are therefore seeking candidates with a unique mix of experience and openness to improvements. 

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.   Exciting opportunity to join our expanding team of Regional Clinical Scientists. The Regional Clinical Scientist will work with the Study Medical Monitor/Study Clinical Scientist and provide scientific and clinical support from ongoing early and late-stage clinical trials with an emphasis on...

As a Local Trial Manager you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.

As a Local Trial Manager you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.

As a Clinical Research Associate you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.

As a Clinical Research Associate you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.

Overview:   This individual performing the services is responsible for Supporting the Project Management of RTSM including (but not limited to) development, UAT testing, administration of documentation and use of RTSM (IWRS) systems for the management of clinical supplies and subjects during the execution