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Pe Global - Galway
Responsibilities. Responsible for the oversight of complaint handling activities for a wide range of business products. Timely submission of US MDR and EU Vigilance Reports to external regulatory agencies. Support the response to any queries received from regulatory agencies in relation to complaint events or post market regulatory reports. Provide oversight of clinical trial activity with respect to complaint handling, and provide appropriate support to the clinical teams as required, including interaction with clinical safety teams. [+]
5 days ago from | Cache