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

We are recruiting experienced UK-based Senior CRAs who are looking for a developmental role - with a strong ability to build relationships at site (involved in problem solving and data review).    You will be partnering with a pharmaceutical company who are consistently delivering on their commitment to improve the lives of people living with severe neurological and immunological conditions. Working in this program you will feel challenged and supported to advance in your professional career while making a truly impact.

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.

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 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 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 (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.

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

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.    You will be part of an innovative and global Biotechnology company, who pride themselves to be one of the world's leading independent biotechnology companies. They focus on areas with unmet medical need with the ambition to help reduce the social and economic burden of disease in society today.

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.

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 play a vital role in providing support to Global Study and Clinical Management Groups and Therapeutic Area Teams by creation of pricing proposals for clinical study budgets, consulting and related agreements.  You will support Finance in the development of study level budget estimates using pricing tools.   You will be part of an innovative and global Biotechnology company, who pride themselves to be one of the world's leading independent biotechnology companies. They focus on areas with unmet medical need with the ambition to help reduce the social and economic burden of disease in society today.

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 one of the world's leading independent biotechnology companies. They focus on areas with unmet medical need with the ambition to help reduce the social and economic burden of disease in society today.

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