As a Clinical Trial Manager you will be leading the Local Study Team(s) (LSTs) at country level to deliver committed components of clinical studies according to agreed resources, budget and timelines complying with Procedural Documents and international guidelines such as ICH-GCP as well as relevant local regulations. In addition to leading LST(s), as the CTM you may perform site monitoring as needed to support the flexible capacity model.

We are currently seeking a Clinical Research Associate to join our diverse and dynamic team at ICON Plc. As a key member of our research department, you will be responsible for overseeing and coordinating clinical trials, ensuring compliance with regulations, and collecting and analyzing critical data.

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

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

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

As a CTM you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence. This role is primarily accountable for the end to end performance and project management for assigned protocols in a country in compliance with ICH/GCP and country regulations, client policies and procedures, quality standards and adverse event reporting requirements internally and externally.

As a CTA / IH CRA you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence. This role is responsible for comprehensive trial and site administration. Under the oversight of the Start Up Lead, the person prepares, collates, distributes and archives clinical documents. The CTA / IH CRA supports clinical supply & non-clinical supply management and ensures timely maintenance of tracking and reporting tools, as...

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

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

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

Manager, Resource Forecasting & Analytics (homebased in UK/Europe) 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. An exciting new role with ICON within within...

CTA Line Manager needed  for a 1-year contract(maternity leave cover), office-based in Cambridge, UK!   We are looking to recruit a CTA Line Manager with solid CTA experience and some management experience.   This is a 1-year contract, with the potential to start as early as November 2025, to enable the...

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

Driving clinical trial excellence through operational and administrative support   As a key member of the Local and Global Study Teams, the CTA ensures seamless coordination of global Phase I–IV clinical trials. Working within GCP, regulatory, and company guidelines, this role supports the delivery of high-quality data for regulatory approvals.

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 Specialist 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 (job title) you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.

Contract Analyst - Clinical Trials Location: Australia (home-based)   As an experienced Contracts Specialist, you will play a key role in improving the lives of patients by accelerating the development of our customers' drugs and devices through innovative solutions.   You will...

Contract Analyst II (Contract & Budget Nego) - Home Based - South Korea   As a (Contract Analyst II) 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...

Clinical Research Associate (Oncology Team) Working Model: Taiwan Client Office based (Flexible WFH)   As a Clinical Research Associate you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.