For a Senior CRA, 3 years + experience is required • College degree in medicine, science, or equivalent • Previous monitoring experience in medium and large -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 (domestic fly and drive) and should possess a valid driving license Benefits of Working in ICON: Our success depends on the knowledge, capabilities and quality of our people. 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: • 2 years + of monitoring experience in phase I-III trials as a CRA (for a CRA II position).