CRA - Clinical Research Associate
hace 4 semanas
About the Role
As a Clinical Research Associate at ICON Plc, you will be working in a large-scale, fast-paced environment alongside a close-knit team of highly qualified CRAs.
Key Responsibilities:
- Identify, select, initiate, and close-out investigational sites for clinical studies in phases II-IV
- Ensure adherence to applicable regulations and principles of ICH-GCP
- Independent, proactive work to set up and monitor studies, complete reports, and maintain documentation
Requirements
- 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
About ICON Plc
Our people are our greatest strength, and the driving force behind our success. At ICON Plc, our focus is to provide you with a comprehensive and competitive total reward package that comprises an excellent level of base pay, variable pay, and recognition programs.
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