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 an In-house Clinical Research Associate, you will be dedicated to one of our global pharmaceutical clients; a prestigious organization, specializing in a niche rare disease, complemented by a pipeline in other therapeutic areas, including oncology. A company that is driving the next generation of patient treatment, where individuals are empowered to work with autonomy and ownership. This is an exciting time to be a part of this new program.

You will be working closely with the wider project team to support the management of investigative sites and ensure that all sites adhere to the requirements and regulations governing Clinical Research.

You will have the opportunity to work on clinical studies at different stages of the project lifecycle and gain a variety of therapeutic experience. The In-house Clinical Research Associate supports with feasibility, study start-up, assisting sites during maintenance and closing out sites.

Key responsibilities in this position include:

• Working within the framework of the study protocol, to assist with the preparation and organization of investigator and study site materials both at a local and international level.
• Working closely with Clinical Team Managers, Start-Up Leads and Clinical Research Associates.
• Working with the wider ICON project team including Regulatory, Contracts and Project Management.
• Performing investigative site recruitment and evaluation.
• Essential document collection, review and maintenance.
• In-house site management activities and ensuring that all study files and documents are current and complete.

You are:

Self-motivated, tenacious and quality focused.

• A life sciences graduate who is keen to begin or develop your career within Clinical Research. We are also keen to review applications from experienced administrators who are interested in working within the Clinical Research industry and clinical site staff looking to work for a CRO.
• Exceptional inter-personal skills, a keen eye for detail and the ability to priorities and multi task.
• The ability to learn new tasks and processes quickly in a fast-paced and dynamic environment.
• Competent with MS Office applications.
• Fluency in English and Netherlands is required.

Benefits of Working in ICON:

Our success depends on the knowledge, capabilities and quality of our people. That’s why we are committed to developing our employees in a continuous learning culture - one where we challenge you with engaging work and where every experience adds to your professional development.

At ICON, our focus is to provide you with a comprehensive and competitive total reward package that comprises, not only an excellent level of base pay, but also a wide range of variable pay and recognition programs. In addition, our best in class employee benefits, supportive policies and wellbeing initiatives are tailored to support you and your family at all stages of your career - both now, and into the future.

ICON, including subsidiaries, is an equal opportunity and inclusive employer and is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.

If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know.