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Independently performs, coordinates and oversees all aspects of the clinical site monitoring services, assessing protocol and regulatory compliance as per Alimentiv’s and sponsor’s standard processes, ICH/GCP guidelines and local regulation. Serves as the primary liaison between
The Clinical Research Regulatory Coordinator is responsible (primarily or in supporting role) for all activities related to the submissions of clinical trials applications in the CTR online platform known as Clinical Trial Information System (CTIS). The
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