CRA II

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 at ICON, you'll work within a large-scale, fast-paced environment alongside a close-knit team of highly qualified CRAs to identify, select, initiate and close-out investigational sites for clinical studies in phases II - IV, ensuring adherence to applicable regulations and principles of ICH-GCP.

The role:
* Independent, proactive work to set up and monitor studies, complete reports and maintain documentation
* Submitting protocol, consent documents for ethics/IRB approval, as well as preparing regulatory submissions
* Balancing sponsor generated queries
* Taking responsibility for study cost efficiency
* Preparation and review of study documentation and feasibility studies for new proposals
* Potential to assist in training and mentoring fellow CRAs

You will need:
* 18 months+ of monitoring experience in phase I-III trials as a CRA
* College degree in medicine, science, or equivalent
* Previous monitoring experience in medium-sized studies, including study start-up and close-out
* Knowledge of ICH-GCP guidelines and ability to review and evaluate medical data
* Excellent written and verbal communication
* Ability to work to tight deadlines
* Availability to travel least 60% of the time (international and domestic -fly and drive) and should possess a valid driving license