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.    The Clinical Trials Assistant (CTA) assists in the coordination and administration of the study activities from the start up to execution and close out, and within the Local Study Team (LST) to ensure quality and consistency of interventional study deliverables to time, cost and quality objectives. -

Role: Clinical Research Associate (12+ months' monitoring experience required) Location: Must be based in the UK, nationwide travel  Fully sponsor dedicated   As a CRA you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.

As a CRA sponsor dedicated, 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 organisation. From molecule to medicine, we advance clinical research providing outsourced services to pharmaceutical, biotechnology, medical device and government and public health organisations. With our patients at the centre of all that we do, we help to accelerate the development of drugs and devices that save lives and improve quality of life. Our people are our greatest strength, are at the core of our culture, and the driving force behind our success. ICON people have a mission to succeed and a passion that ensures what we do, we do well.

As a Senior Contract Analyst 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.

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

At ICON, we are passionate about transforming clinical development and driving better outcomes for patients through innovation. We are currently seeking an Advanced Solutions Designer to join our global team. This role sits at the intersection of user experience, data, and technology—helping to shape the future of decision-making in healthcare and life sciences.   You will work fully outsourced to a Top Pharmaceutical sponsor company in this role. With a user-first approach, you will help build intuitive, scalable solutions that reduce the complexity of data interpretation—ensuring that insights lead to action.

As a CRA   you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence. Identify, select, initiate and closeout appropriate investigational sites for clinical studies. • Monitor those sites in order to ensure that studies are carried out according to the study protocol and in accordance with ICON SOPs/WPs applicable regulations and the principles of ICH-GCP.

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

We are currently seeking a Clinical Research Associate to join our diverse and dynamic team. As a Clinical Research Associate at ICON, you will play a pivotal role in designing and analyzing clinical trials, interpreting complex medical data, and contributing to the advancement of innovative treatments and therapies.   This role is fully sponsor dedicated and you would be working in an FSP model. Within this program you will...

As a Manager, Regulatory CMC (lifecycle management) you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.   We are seeking 2 roles within our Regulatory CMC team - CMC Life Cycle Management experience for Drug substance and Drug product is essential for this role. -

As a CRA 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 organisation. From molecule to medicine, we advance clinical research providing outsourced services to pharmaceutical, biotechnology, medical device and government and public health organisations. With our patients at the centre of all that we do, we help to accelerate the development of drugs and devices that save lives and improve quality of life. Our people are our greatest strength, are at the core of our culture, and the driving force behind our success. ICON people have a mission to succeed and a passion that ensures what we do, we do well.

As a CTA (Payments), you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.

(Sr.) CRA I or II, Home-based, South Korea   As a (Sr.) CRA I or II 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.

Regional CTA submission manager (EU CTR) - Homebased in UK or Europe An exciting new role with ICON within our regulatory team working on high profile Pharma projects with a client with which ICON shares a culture of innovation, flexibility and a common vision of bringing life-improving drugs to market. The Regional CTA Submission Manager (CTA-SM) is accountable for working with contributing to business lines to lead operational submissions execution for...