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Clinical Research Monitor




Responsibilities:Monitors progress of clinical trials at the site level or headquarters and ensures that they are conducted, recorded and reported in accordance with the protocol, standard operating procedures (SOP), good clinical practices (GCP), and other applicable regulatory requirements.Develops and maintains liaison with clinical investigators, clinical research organizations (CRO), affiliated hospitals, and research institutions to initiate and expedite clinical studies on products that have investigational new drug or medical devices approval.Reviews adverse event cases with investigators, determines and monitors time, budget, schedules, prepares study documents, and issues status reports.

Posted 23 days ago

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