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

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

We currently have an exciting new opportunity for an experienced Global Clinical Project Manager to join a successful sponsor dedicated program. We are looking for a Global Clinical Project Manager which is a business-critical role within Study Management, BioPharmaceuticals Clinical Operations, whose main accountability is the delivery of clinical studies.   The Global Clinical Project Manager is responsible for leading a cross-functional study team and for providing the team with direction and guidance to enable successful study delivery....

We are currently seeking a Site Activation Lead to join our diverse and dynamic team. As a Site Activation Lead at ICON, you will advance clinical trial start-up activities by understanding client objectives and assisting in the development of the plan for country and site distribution. We pride ourselves on our amazing company culture, where we work as one team to achieve industry-leading results.

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

As a Senior Clinical Data Science Lead you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence. En tant que responsable principal de la science des données cliniques, vous rejoindrez l'organisation de recherche clinique la...

We are currently seeking a Validation Engineer to join our diverse and dynamic team. In this role at ICON, you will be responsible for executing validation activities for equipment, systems, and processes in clinical operations, ensuring compliance with regulatory standards and quality assurance. Your technical expertise and analytical skills will be crucial in maintaining the integrity and efficiency of our validation processes.

As a Lead Clinical Data Science Programmer you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.   We are seeking a highly skilled Lead Clinical Data Science Programmer to support our Global Development Data Management team by developing and maintaining standard and custom clinical data reports and tools across multiple platforms. This role is critical to ensuring high data quality, regulatory compliance, and operational excellence in clinical data oversight.

As a Senior Lead Clinical Data Science Programmer you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence. We are looking for a strategic and technically skilled Senior Lead Clinical Data Science Programmer to elevate our data quality and monitoring processes. This role is crucial in driving clinical data validation, building scalable data pipelines, and delivering impactful reports and insights to cross-functional clinical teams. You will work across various data modalities and platforms, helping shape the future of data integrity and innovation in clinical development.

As a Senior Clinical System Lead you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence. We are seeking a highly motivated Clinical Data Ingestion & Management Specialist to drive the participant data journey from source identification to ingestion, harmonization, and integration into our clinical data ecosystem. This role bridges technical and clinical teams, providing guidance on data ingestion strategies, vendor capabilities, and ensuring data quality and compliance throughout the study lifecycle.

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

As a Senior Clinical Trial Transparency Associate you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.   You will oversee and execute the clinical transparency (i.e., registration, updates and/or results disclosure) or public disclosure processes for assigned studies and/or...

As an Associate Project manager at ICON, you will play a pivotal role in supporting the coordination and management of clinical trials, contributing to the design, analysis, and advancement of treatments and therapies.

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

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

Investigator Contracts Lead is 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 ICL or pCRO and collaborating with other lines to plan site contracting timelines though start-up.

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

The role defines and facilitates the participant data journey, identifying participant data sources, transport methods, ingestion to client's ecosystem and mitigating potential challenges to ensure understanding, consistency and integrity of the participant data. The role will collaborate with technical and clinical teams across client's to define participant data requirements and challenges to provide short- and long-term solutions and be a subject matter expert within data management and statistics to facilitate effective data use and risk mitigation.