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Job Description & How to Apply Below
A leading clinical research organization is seeking a Clinical Research Associate with oncology experience to manage assigned study sites throughout the UK. You will be responsible for site selection, monitoring compliance with clinical trial protocols, and ensuring high-quality data delivery. The ideal candidate will have two years of experience in the pharmaceutical or CRO industry, along with a solid understanding of the drug development process and GCP standards.
Frequent travel, both domestic and potentially international, is a key part of this role.
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Position Requirements
10+ Years
work experience
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