Clinical Research Associate I at ICON will deliver clinical trial monitoring and regulatory compliance work across sponsor-dedicated programmes. The role involves coordinating study setup, managing queries, maintaining documentation, and ensuring patient safety through adherence to GCP guidelines and protocols.

Responsibilities

- Coordinate study setup and monitoring activities; prepare accurate status reports and study documentation
- Execute sponsor-generated queries and manage study cost efficiency
- Develop and maintain collaborative relationships with clinical investigators and site staff
- Ensure compliance with regulatory requirements and ICON procedures to maintain patient safety

Requirements

- University degree in medicine, science, or equivalent field
- Knowledge of ICH-GCP guidelines and ability to review medical data
- Fluent written and verbal English communication
- Strong interpersonal skills and ability to manage queries promptly
- Relevant clinical trial monitoring experience
- Willingness to travel approximately 60%

📌 Clinical Research Associate 1 (España)
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📍 España