Job Title: (Sr.) CTA Working model: Office based in global pharma, Taiwan, Taipei office   If you are seeking a career where you can truly make a difference in the lives of others, working closely together with the top minds in the pharmaceutical Industry, then here is your chance. We are hiring a "Clinical Trial Assistant" to work closely with our client, a leading pharmaceutical company.

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 (Senior 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 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 Clinical Research Associate II at ICON, you’ll work within a large-scale, fast-paced environment alongside a close-knit team of highly qualified CRAs to identify, select, initiate and close-out investigational sites for clinical studies in phases II – IV, ensuring adherence...

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

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

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

(Senior) Clinical Trial Assistant Location: Homebased - Belgium   As (Senior) Clinical Trial Assistant, you will be joining the world's largest & most comprehensive clinical research organisation, powered by healthcare intelligence.   

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

An additional UK home-based Oncology Clinical Project Manager is required to manage sites (with some CRA Line Management responsibilities) within the UK region.   You will be partnering with a well-known global pharmaceutical company with a strong portfolio in cancer, cardiovascular, gastrointestinal, infection, neuroscience, respiratory and inflammation medicines.  

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

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

Site Management Associate I, Home-Based, South Korea   As a (Site Management Associate I) 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...

As a Clinical Study Administrator (CSA) , you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence. The Clinical Study Administrator (CSA) 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.

The Study Start-Up Manager is accountable for study planning, SSU activities and activation deliverables of assigned projects in compliance with client processes, GCP/ICH and regulatory requirements in a standalone country, OPC (operating country) or satellite country. Leads all SSU activities of assigned projects in close collaboration with Feasibility Manager and Site Partnership Manager as well as the global study team.  In satellite countries acts as primary back-up and deputy of the country manager.

Role: Clinical Trial Associate  Location:Sydney, hybrid   As a Clinical Trial Associate you will have the opportunity to work with one of the world’s leading pharma & biotech companies, helping them advance new drugs and devices.  

We are currently seeking a Study Operations Manager to join our diverse and dynamic team. As a Project Manager at ICON, you will be responsible for leading and coordinating project activities, ensuring that projects are delivered on time, within budget, and to the highest quality standards. Your role will involve overseeing all aspects of project execution, from planning and resource management to stakeholder communication and risk mitigation.

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