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

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

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

As a 2nd shift Warehouse Technician you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.   Monday - Friday - 2nd Shift - 2PM to 10:30PM  This role is 5 days weekly onsite in our facility in West Point, PA (19486). 

As a Warehouse Technician you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.   First Shift, Monday - Friday - 2nd Shift 2PM to 10 PM  This role is 5 days weekly onsite in our facility in West Point, PA (19486). 

As a Warehouse Technician you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.   First Shift, Monday - Friday - 2nd Shift 2PM to 10 PM  This role is 5 days weekly onsite in our facility in West Point, PA (19486). 

As a Warehouse Technician you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.   First Shift, Monday - Friday  - 2nd Shit 2 PM to 10 PM  This role is 5 days weekly onsite in our facility in West Point, PA (19486). 

This Global Risk Management & Safety Surveillance (GRMSS) Scientist collaborates with the GRMSS Physicians and GRMSS Scientists to characterize the evolving clinical and post-marketing safety profiles for investigational drugs and/or products, based on analysis of aggregate data sets from internal or external sources and the medical literature.  This entails drafting, reviewing, and refining portions of periodic aggregate safety reports (including DSURs, PADERs/PAERs).  The GRMSS Scientist performs the signal detection activities and review process for clinical data, including signal detection, evaluation, and verification; potential sources of...

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

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

As Clincial Research Lead (Site Engagement) 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.   You will be engaged in a wide range of...

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

As a Principal R Programmer 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 Director, Regulatory Affairs.    This is an exciting opportunity for a strategic leader passionate about clinical development and regulatory submissions. If you thrive in a fast-paced, global environment and want to shape the future of oncology...

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 advance and improve patients’ lives. Our ‘Own It’ culture is driven by four key values that bring us together as individuals and set us apart as an organization: Accountability & Delivery, Collaboration, Partnership and Integrity. We want to be the Clinical Research Organization that delivers excellence to our clients and to patients at every...