As a (job title) 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 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 Clinical Research Associate you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.   You will be working alongside a world-leading pharmaceutical company. This 19- year partnership is focused on leveraging cutting-edge science to

A Clinical Research Associate is a professional who contributes to accelerated drug/device/outcomes research through independent monitoring of studies to ensure patient safety and data integrity.   You will be joining a program takes an extensive co-monitoring approach that enables a supportive and collaborative work environment. Frequent, consistent communication, both internally and with our client, positions our program to be closely aligned on our shared goals. mprehensive clinical research organisation, powered by...

We're hiring a Contract Analyst I for a client-dedicated, home-based role in France.

As a Clinical Trial Assitant based in the Netherlands you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.  

As a Study Start Up Associate you will play a key player in differentiating ICON by accelerating site start-up through effective execution of regulatory approvals and of site contracts ensuring sites are ready to enrol patients as quickly as possible. This role may serve as Site Activation Lead when appropriate. Ensuring timely collection of critical documents in order to begin patient enrolment. Critical path to study initiation.

As a Clinical Research Coordinator (SMAII) located in the area Eindhoven you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.

We are hiring a Clinical Research Lead, sponsor dedicated in the area Utrecht  

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

As a Study Start Up Manager 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 SSU 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 Contract Analyst I, you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.

Role: Clinical Research Associate (12+ months' monitoring and Oncology 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 CDC you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.

Senior CRA-Home Based-South Korea   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...

The Senior Contract Associate is responsible for all aspects of preparation, negotiation, and execution of required site/investigator contracts. The Senior Contract Associate assumes responsibility on quality deliverables throughout the conduct of the study with a concentration on site/investigator contracts during Site Start Up and up to Site initiation.