Senior CRA

at  Icon plc

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 for Medical Devices and Diagnostics Research at ICON, you’ll work within a large-scale, fast-paced environment alongside a close-knit team of highly qualified CRAs and medical devices experts to identify, select, initiate and close-out investigational sites for pre and post market studies, ensuring adherence to applicable regulations and principles of ICH-GCP. We pride ourselves on our amazing company culture, where we work as one team to achieve industry-leading results.

The Role:

• Working independently and actively to coordinate activities to set up and monitor a study, completing accurate study status reports and maintaining study documentation
• Ensuring safety and rights of patients is maintained throughout the study.
• Working solely on Medical Devices or In Vitro Diagnostic studies, in various phases (First in Man, Registry, Post-market Follow-up…) and in various therapeutics areas (cardiovascular, neurology, oncology, Ophthalmology, Orthopaedics….)
• Ensuring close and regular site contact management by developing strong relationship with site staff and site investigators
• Balancing sponsor generated queries efficiently and responsible for study cost-effectiveness
• Dependent on level of experience you may assist in training and mentoring less expert CRA’s and/or lead CRA’s working on international projects

• Working independently and actively to coordinate activities to set up and monitor a study, completing accurate study status reports and maintaining study documentation
• Ensuring safety and rights of patients is maintained throughout the study.
• Working solely on Medical Devices or In Vitro Diagnostic studies, in various phases (First in Man, Registry, Post-market Follow-up…) and in various therapeutics areas (cardiovascular, neurology, oncology, Ophthalmology, Orthopaedics….)
• Ensuring close and regular site contact management by developing strong relationship with site staff and site investigators
• Balancing sponsor generated queries efficiently and responsible for study cost-effectiveness
• Dependent on level of experience you may assist in training and mentoring less expert CRA’s and/or lead CRA’s working on international project