(Senior) Clinical Research Associate/ Clinical Research Associate II
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About the job
As a (Senior) Clinical Research Associate at ICON, you will embark on an exciting journey in the world of clinical trials, playing a pivotal role in advancing innovative treatments. Your expertise will help shape the future of clinical development, ensuring patient safety and data integrity. Join a diverse and dynamic team that values collaboration and innovation, and be part of a mission that truly makes a difference.
You'll be responsible for
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Conducting site visits
Conducting site qualification, initiation, monitoring, and close-out visits for clinical trials to ensure protocol compliance and patient safety.🤝
Collaborating with investigators
Collaborating with investigators and site staff to facilitate smooth study conduct and maintain high-quality clinical data.📄
Preparing study documentation
Contributing to the preparation and review of study documentation, including protocols and clinical study reports.Key criteria
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Bachelor's degree in a scientific field
Possession of a relevant degree for clinical research.View
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1.5+ years as a Clinical Research Associate
Demonstrated experience in clinical trial monitoring.View
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Knowledge of clinical trial regulations
In-depth understanding of ICH-GCP guidelines and processes.View
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