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.

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.

Responsible for ensuring high quality medical review of phase I-III clinical trial data in the field of oncology, neurology and immunology, in compliance with GCP/ICH and regulatory requirements. Provide high quality, timely and diligent clinical data review to ensure adequate data quality for the successful completion of clinical trials and regulatory submissions.

Study Start-Up Project Manager, Home-Based, South Korea   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

Clinical Research Associate II or Senior Clinical Research Associate Location: Melbourne/ home-based    As a Clinical Research Associate, 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....

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 (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.  

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.  

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.

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 member of the Study Start Up Team, you will play an integral role in making sure that physicians at our research sites are prepared to start the trial of investigational, new pharmaceutical and biological products for clinical trials at their local practices.

Title - Clinical Research Associate  Location - UK, nationwide travel  Sponsor dedicated    As a CRA you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.

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 Local Trial Manager (LTM) you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence. 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. As a LTM you will be tthe primary point of contact to lead, manage and co-ordinate the conduct of clinical trials from study start-up to close out at a country level in accordance with ICH-GCP and other applicable local regulation. You will maintain the...

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

As a Clinical Research Associate (CRA) you will coordinate all aspects of the clinical monitoring and site management process in accordance with regulatory guidelines, local regulations and standard operating procedures. In this role you will be a decision maker, solving problems independently or as part of the client and ICON team. You will be managing competing priorities, supporting the on-site team, ensuring investigators follow the clinical trial protocol, providing training, and most importantly, motivating the team to ensure high quality results.

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

As Clinical Site Manager you will be responsible for maximizing site performance and site engagement in our client conducted clinical studies, as well as leveraging strong clinical operational and therapeutic expertise to support execution of the clinical studies.   ICON plc is a world-leading healthcare intelligence and clinical research organisation. From molecule to...