The Clinical Research Associate (CRA) monitors the progress of clinical studies at investigative sites or remotely, ensuring clinical trials are conducted, recorded, and reported in accordance with the protocol, standard operating procedures (SOPs), International Conference on Harmonization Good Clinical Practices (ICH-GCP) and all applicable regulatory requirements.

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 partnering with one of our global pharmaceutical clients; a company that is advancing the development of new medicines, biologic therapies and vaccines for many of the world’s most challenging diseases including cancer, cardio-metabolic diseases, Alzheimer’s  and infectious  diseases.  Be ready to work in a solid partnership and an...

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 partnering with one of our global pharmaceutical clients; a company that is advancing the development of new medicines, biologic therapies and vaccines for many of the world’s most challenging diseases including cancer, cardio-metabolic diseases, Alzheimer’s  and infectious  diseases.  Be ready to work in a solid partnership and an...

Clinical Research Associate (Oncology)  - Homebased- South Korea   You will play a vital client facing line management role, embedded in our clients business. You will be responsible for the management of day to day clinical trial quality activities, ensuring everyone is well-trained on ICON standard processes, and promoting efficiency, quality, and timeliness in project work.

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 Medical Director you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.   Medical Director, Clinical Development Sciences Hematology may lead the clinical sub-team or support the clinical sub-team and the global program team to build global clinical development plans and contributes to the development of asset level and therapeutic area strategies. Responsible for overseeing the clinical development strategy development and execution for 1 program, leading the...

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 CRA based in the Netherlands (the Hague area) you will coordinate all aspects of the...

This role is only open to Senior CRA's and is Paris based, 3 days ICON office based in Puteaux and 2 days remote.   As an SSU CRA, you will be responsible for coordinating and overseeing the study start-up phase of clinical trials. You will ensure all regulatory and ethical submissions are completed efficiently and to the highest standards. This role is primarily office-based in Paris with minimal travel requirements.

As an Associate Project manager at ICON, you will play a pivotal role in supporting the coordination and management of clinical trials, contributing to the design, analysis, and advancement of treatments and therapies.

Principal CRA (Lead CRA Role), Home-Based, Bangkok Thailand   As a (Principal CRA) you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.

We are hiring a Clinical Trial Manager, sponsor dedicated (Eindhoven area)Position Summary: The Clinical Trial  Manager plays a key role in ensuring high-quality clinical study execution across all active clinical research initiatives. You will lead, support, and manage clinical studies to generate critical clinical evidence, aligned with business goals and regulatory compliance requirements. The role requires close collaboration with cross-functional teams, effective use of...

🚀 Op zoek naar een nieuwe uitdaging als CRA?   Werken voor één sponsor en toch blijven groeien? 👉 Dan is dit jouw kans! ICON plc is op zoek naar een ervaren Clinical Research Associate (CRA). Samen bepalen we welk level het best aansluit bij jouw ervaring. Je werkt exclusief voor...

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 hiring a Clinical Trial Coordinator (CTA) within our Strategic Solutions team!

We currently have an exciting new opportunity for an experienced Global Clinical Project Manager within the Oncology team to join a successful sponsor dedicated program. We are looking for a Global Clinical Project Manager which is a business-critical role within Study Management, BioPharmaceuticals Clinical Operations, whose main accountability is the project delivery of clinical studies.   The Global Clinical Project Manager is responsible for leading a cross-functional study team and for providing the team with direction and guidance to enable...

As a Clinical Development Scientist  you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.   At this role you will lead a clinical sub-team or support the clinical sub-team and the global program team to build global clinical development plans and contribute to the development of asset level and therapeutic area strategies. Responsible for overseeing the clinical development strategy development and execution for one or several projects,...

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

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

The Clinical Research Associate (CRA) monitors the progress of clinical studies at investigative sites or remotely, ensuring clinical trials are conducted, recorded, and reported in accordance with the protocol, standard operating procedures (SOPs), International Conference on Harmonization Good Clinical Practices (ICH-GCP) and all applicable regulatory requirements.