We offer a full range of consulting, clinical development and commercialisation services from a global network of offices in 46 countries
Since our foundation in Dublin, Ireland in 1990, our mission has been to help our clients to accelerate the development of drugs and devices that save lives and improve quality of life.
We are a global provider of co...
Read more about this company
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 in Local language and English
Gmail
Yahoomail