As a Senior Biostatistician 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 created a strong heritage of delivering innovative treatments and preventive medicines globally.

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 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 Senior Biostatistician I 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 Feasibility Lead 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.

As a CRA II 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.

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.

Job title: Associate Project Manager Working location: Taipei, Taiwan, Client office based   Providing innovative solutions for our clients is what we do. But innovation just for the sake of innovation isn’t why we do it. Side-by-side with...

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.  

ICON’s FSP group is recruiting a handful of additional UK-based Global Trial Managers to augment their existing GTM team and manage a diverse range of client protocols. You will be partnered with an innovative global biotechnology company focused on areas of unmet medical need, with the ambition to reduce the social and economic burden of disease in today’s society. -

As a Senior CRA / Clinical Site Manager you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence. You’ll utilise your extensive therapeutic knowledge in Oncology to oversee uniquely-focused clinical studies. Working at the core of clinical research, you’ll be exposed to cutting-edge protocols and experience a dedicated partnership with your team like never before.