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

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

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

As a SCRA 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....

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

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

We are currently seeking a Manager, CTM (Clinical Trial Management) to join our diverse and dynamic team. As the Manager of CTM at ICON, you will play a pivotal role in overseeing the planning and execution of clinical trials, ensuring that they are conducted efficiently and in compliance with regulatory standards. Your leadership will be crucial in driving the success of our clinical programs and supporting the advancement of innovative therapies.

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

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

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 Clinical Trial Assistant you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.   This CTA role is dedicated to one client and is partially office based 

The Lead Clinical Data Science Programmer will be responsible for effectively supporting the Global Development Data Management organization by creating and maintaining a global library of standard data management reports, listings, metrics, and graphs to drive data quality and support data management oversight activities. The Senior Reports Developer will support clinical study teams to use defined standard DM reports on different platforms including but not limited to JReview, Business Objects, SAS and Spotfire.

The role involves being a Senior Lead clinical data science programmer in the Clinical Data Management area, focusing on enhancing data review and cleaning processes with innovative reports. It entails creating and implementing study- specific data validation procedures and reports, managing the connection to varied data sources, and ensuring efficient scheduling, monitoring, and maintenance on the Clinical Data platform. The role requires detailing key handling requirements for scalable data management methods, and deriving study-specific monitoring and validati reports based on clinical protocols and amendments. Ultimately, this position aims to advance clinical data management and informatics by improving data...

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.

Clinical Research Associate Working Model: Hong Kong Client Office based   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 Clinical Contracts Assoicate you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.