CRA II or Senior CRA at ICON plc

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 
• Submission of protocol, consent documents for ethics/IRB approval and assist in preparing regulatory submissions as requested 
• Balancing sponsor generated queries efficiently, manage and support sites and responsible for study cost-effectiveness 
• Dependent on level of experience you may assist in training and mentoring less expert CRA’s

To be successful in the role, you will have:

• At least 12 months of independent, on-site monitoring experience
• Knowledge of ICG GCP guidelines and expertise to review and evaluate medical data
• Great command of the local language and) English (command of any other languages will be considered an advantage
• Ability to produce accurate work to tight deadlines within a pressurized environment
• You will be asked to travel around 60% of the time domestically (on rare occasions internationally) and should possess a valid driving license