Icon plc is a world-leading healthcare intelligence and clinical research organisationFrom 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 successIcon people have a mission to succeed and a passion that ensures what we do, we do well.
Responsibilities
As an in-house clinical research associate 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 researchYou will receive comprehensive training which will enable you to learn, before moving to work on your own studies with continuing support, training and mentorship.
You will have the opportunity to work on clinical studies at different stages of the project lifecycle and gain a variety of therapeutic experienceThe 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 organisation 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 pra 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.
Qualifications
You are:
Self-motivated, tenacious and quality focused.
Here at icon we want our employees to succeed and ensure that they are set up for this success through constant training, development and supportTo enable success in this position we are seeking:
A life sciences graduate who is keen to begin or develop your career within clinical researchWe 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 prioritise and multi task.
The ability to learn new tasks and processes quickly in a fast-paced and dynamic environment.
Competent with ms office applications.
Benefits of working in icon:
Our success depends on the knowledge, capabilities and quality of our peopleThat’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 programsIn 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 harassmentAll 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.
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