Cra Ii

**Overview**:
- As a single sponsor dedicated Clinical Research Associate at ICON, you will be partnering with a well-known global pharmaceutical company, where you will be responsible for Norway. You will have an opportunity to work in a solid partnership and an environment driven by innovation and continuous improvement. This program is for you if you are looking for an environment where people feel they belong and are empowered to reach their full potential, perform at their best and make a valued contribution to saving lives.
**Responsibilities**:
**What you will be doing**:
- 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 proposa...