Parexel
A global biopharmaceutical services firm seeks a Senior Clinical Research Associate to manage site monitoring and ensure compliance with clinical trial regulations. The candidate will be responsible for site management from activation to close-out, focusing on quality and patient safety. A Bachelor's degree in life sciences and a minimum of 3 years of experience in clinical monitoring, preferably in Oncology, are required. This role also involves traveling 60-80% of the time and being fluent in English and local languages.
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