The Clinical Trial Start-up Associate  ensures that patients will have access to our clinical trials with the aim of making life better for our patients. The Associate is accountable for obtaining all approvals (Competent Authority and Ethical Review Board) to run the trial in the EMEA and AMERIT Regions. The Associate will also have responsibility to ensure the investigator sites meet the requirement to enroll the study participants in the clinical trial and support maintenance and closeout activities. The Associate will ensure inspection readiness through a complete, accurate and readily available Trial Master File. Additional local responsibilities may be required...

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 Senior CRA in Israel 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 the Project Manager you're responsible for study management aspects of assigned studies of limited complexity (e.g. single country, a small number of countries/sites) or manage a unique part of a larger study (e.g. recruitment and retention).

As a CRA in Finland you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare and assigned to a single sponsor.

As a CRA in Denmark you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare and assigned to a single sponsor.

As a CRA in Sweden you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare and assigned to a single sponsor.

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

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

As a Graduate Pharmacovigilance Assocaite you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.   You will be partnering with a pharmaceutical company committed to discovering and developing treatments that improve and save people´s lives. Working in this program you will feel challenged and supported to advance in your professional career while making a truly impact.

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

Regulatory Affairs Specialist, Seoul, South Korea   You will have an opportunity to work in a solid partnership and an environment driven by innovation and continuous improvement. This program is for you if you are looking for an environment where people feel they belong and are empowered to reach their full potential, perform at their best and make a valued contribution to saving lives.  

As a CRA you will be joining the world’s largest & most comprehensive clinical research organization, powered by healthcare intelligence.   En tant qu’ARC (Associé(e) de recherche clinique), vous rejoindrez la plus grande et la plus complète organisation de recherche clinique au monde, propulsée par l’intelligence en santé.  

We are currently seeking a Senior Project Manager to join our diverse and dynamic team. As a Senior Project Manager at ICON, you will be responsible for leading and managing projects, ensuring successful execution and delivery of project objectives.

We are currently seeking a Principal Auditor Quality Assurance to join our diverse and dynamic team. As a Principal Auditor Quality Assurance at ICON, you will play a pivotal role in ensuring the quality and compliance of clinical trials, interpreting regulatory requirements, and contributing to the advancement of inNvative treatments and therapies.

As a C-SOM you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.   En tant que C-SOM, vous rejoindrez la plus grande et la plus complète organisation de recherche clinique au monde, alimentée par l'intelligence en matière de santé.

As a Site Management Liaison you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.   You will be joining one of the global healthcare leaders that has been discovering and developing medicines and treatments for well over a century. You will be part of a global team that is committed to make life better for people around the world. We share a vision of bringing treatment and medicine to millions alongside develop...

We are growing our Team and hiring a UK-homebased Clinical Trial Manager to work as a Clinical Risk Manager within our global study team. The successful candidate will need to start in September or October.   - Are you an experienced Clinical Trial Manager with strong influencing and leadership capabilities? - Can you navigate cross-functional environments and drive risk management strategies effectively?

We are looking for a candidate experience in budget and contract negotiations for clinical trials with Fluent Ukraine and French Langugage knowledge  The mission of the Trial Capabilities Centre (TCC) Business Operations group is to provide clinical trial site budget and contract negotiations, purchase order creation, and payment support for clinical trial and medical research consulting agreements with...

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 the Project Manager you're responsible for study management aspects of assigned studies of limited complexity (e.g. single country, a small number of countries/sites) or manage a unique part of a larger study (e.g. recruitment and retention).

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 the Project Manager you're responsible for study management aspects of assigned studies of limited complexity (e.g. single country, a small number of countries/sites) or manage a unique part of a larger study (e.g. recruitment and retention).