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 looking for a Sr. CRA with Oncology experience located in the Mid-West Region!! 

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 looking for a Sr. CRA with Oncology experience located in the NorthEast Region!! 

As a Clinical Research Associate, you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence. We are looking for an Oncology CRA in the Northeast Region!! 

  As a Clinical Adjudication Project Lead, you will play a key role in improving the lives of patients by accelerating the development of our customers ' drugs and devices through innovative solutions.   You will be a dedicated resource to one of our clients, embedded in their working environment, systems, and processes.

  As a Clinical Adjudication Project Lead, you will play a key role in improving the lives of patients by accelerating the development of our customers ' drugs and devices through innovative solutions.   You will be a dedicated resource to one of our clients, embedded in their working environment, systems, and processes.

  As a Clinical Adjudication Project Lead, you will play a key role in improving the lives of patients by accelerating the development of our customers ' drugs and devices through innovative solutions.   You will be a dedicated resource to one of our clients, embedded in their working environment, systems, and processes.

ICON is looking for a Study start-up focused CTA  to support one of our FSP clients!! 

As a Sr. CRA 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 Medical/Clinical Data Reviewer you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.

As a CRA you will be joining the world’s largest & most comprehensive clinical research organization, powered by healthcare intelligence. We are currently looking for a CRA II with Late Phase ONC/HEM experience for one of our FSP programs! 

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

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

As a Clinical Data Reviewer 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 organization, powered by healthcare intelligence.

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

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

We are looking for a CTL&D Analyst to provide support to CTL&D TA Leads for protocol specific training planning within assigned therapeutic area(s).  Service/deliverables include support to deliver on protocol specific training related processes, including, but not limited to development / documentation of the Global Protocol Training Plan (GPTP) for each protocol assigned.