Clinical Research Professional
3 days ago
Clinical Research Professional
At ICON, you will be part of a world-class team working on cutting-edge clinical research projects. As a Clinical Research Associate, your primary responsibility will be site monitoring and management.
- You will work closely with investigators to ensure the successful management of sites throughout the study lifecycle.
- In accordance with ICH-GCP guidelines and internal Standard Operating Procedures, you will monitor and manage sites to ensure compliance.
What You Need To Succeed:
- Bachelor's degree or above in a life science or related field.
- More than 1 year of global oncology study experience as a CRA.
- Proven track record of site monitoring and management.
- Excellent communication and organizational skills.
Why Choose ICON?
We offer a comprehensive and competitive total reward package that includes an excellent base pay, variable pay, and recognition programs. Our best-in-class employee benefits and supportive policies are designed to support you and your family at all stages of your career.
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