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 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 to...

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 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 to...

As a Project Manager/ Country Study Operation Manager you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence. Working location: Homebased, Taiwan

As a Clinical Research Associate, you will be fully dedicated to one of our global pharmaceutical partners — a collaboration built on shared values of innovation, flexibility, and a joint mission to bring life-changing treatments to patients faster.   This is your opportunity to be part of an exclusive, high-impact program where you can lead by example and shape the standard for clinical excellence.   -

As a Clinical Trial Assistant you will be dedicated to one of our global pharmaceutical clients; with whom ICON shares a culture of innovation, flexibility and a common vision of bringing life-improving drugs to market. Leading by example, you can set the standard of excellence and enjoy a challenging career in our exclusive programs.   We are currently looking for a Clinical Trial...

Jot Title: Site Care Partner Working location: client office based (Flexible WFH) Sponsor: Top 10 Global pharma   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.

Role: Clinical Research Associate II/ Senior Clinical Research Associate FSP Location: Melbourne/ Sydney/ Brisbane/ Adelaide (home-based)   As an experienced Clinical Research Associate, you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.  

Oncology (Sr.)CRA II, Home-Based, South Korea   As a (CRA II/SCRA) you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence. You will be partnering with one of the worlds premier Biopharmaceutical companies. Working across a vast portfolio of medicines and vaccines this company has, over centuries...

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

Contract/Budget Role 1. Location: Home-Based, South Korea 2. Location: Taipei office based with flexible WFH   As a (Contract Analyst I) you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.

As a single sponsor dedicated Clinical Research Associate at ICON, you will be partnering with a well-known global pharmaceutical company, where you will be responsible for Sweden. 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 Data Management Reviewer you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence. This is an hybrid role and it requires 3 days per week at the client’s office and 2 days working from home. Office location: Diegem (Brussels area), Belgium OR Warsaw, Poland

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

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...

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

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

Role: Clinical Research Associate (12+ months' monitoring experience required) Location: Must be based in Switzerland nationwide travel  Must be fluent in French Fully sponsor dedicated   As a CRA you will...

As a Contract Analyst you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence. You will be responsible for direct site-facing contract and budget negotiations thought contract execution with assigned clinical investigator sites including initial agreements and amendments and oversight of other contracting professionals on assigned studies. This also includes managing the Per-Subject Cost (PSC) process for assigned studies, managing escalation and resolution for budget and non-legal term issues from other...

As a Clinical Trial Transparency Associate you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.   In this role you will oversee and coordinate redaction activities across multiple delivery units, Familiarity with clinical trial and submission documents is required.

As a Data Management Developer you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence. This is an hybrid role and it requires 3 days per week at the client’s office and 2 days working from home. Office location: Diegem (Brussels area), Belgium OR Warsaw, Poland