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As a Clinical Quality Manager you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.
Under the guidance of the Regional Director, Clinical Quality Management, the Clinical Quality Manager oversees all CQM activities in the respective country/cluster.
The role requires the ability to properly implement local/global processes/procedures, to identify opportunities for process improvement and to...
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...
As a (CRA) you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.
As a (CRA II, SCRA) you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.
As a (Site Activation Lead) you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.
Clinical Research Associate – Johannesburg, South Africa
As a Clinical Research Associate, you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence. You will be a part of ICON Strategic Solutions, embedded to a sponsor.
We believe our Clinical Operations team is second to none. You will receive the support you need to develop personally and professionally and...
Senior Clinical Trial Transparency Associate is responsible for CTT deliverables, the role is single sponsor dedicated.
The role can be based in Eastern Europe
(Sr) Payment Analyst
Location: Taiwan, Taipei
As Payment Analyst, you will be joining the world's largest & most comprehensive clinical research organisation, powered by healthcare intelligence.
The Study Start Up. Assocate II, collect, prepare, review, approve, process and track regulatory and site level critical documents required for study site activation in accordance with ICON SOPs/WPs, Sponsor SOPs, applicable country regulations/guidelines and the principles of ICH/GCP.
Embrace and contribute to ICON’s culture of quality and process improvement with a focus on enhancing processes, systems and tools, adding value to our business and meeting or exceeding client needs.
As a Senior Clinical Data Science Lead - Data Management you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.
Regulatory Affairs Manager- (EU CTR) Homebased in UK/Ireland Only
Due to recent success within one our Innovative Biotech Clients I am recruiting for a Regulatory Affairs manager at ICON - Working in a client-dedicated yet fully embedded role ICON’s Regulatory Strategy group, you will lead or contribute to the development and execution of the drug development strategy of our client’s new therapeutics.
Responsible for outsourcing and facilitation of the delivery of (currently only preclinical) CPSS aspects of drug projects. Monitors that these activities fall within agreed time, budget and quality. Supports the project team by providing guidance and advice on tools, processes and outsourcing. Able to solve day to day issues problems within own area of projects.
We are looking to recruit an Investigator Pricing Analyst to join our global team performing clinical pricing & payments senior associate tasks. The role is fully homebased in the UK!
You will...
As a Principal Medical Writer 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.
Clinical Trial Assistant
Location: Office-based / Hybrid, Sydney (Australia)
As Clinical Trial Assistant, you will be joining the world's largest & most comprehensive clinical research organization, powered by healthcare intelligence. You will be part of an innovative and global Biotechnology company, who pride themselves to be...
As a Clinical Study Associate you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.
Clinical Study Associate
Taiwan Office based
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.