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Work is toBe fully competent to perform all steps within the case-handling process from triage through to QRE quality review for cases of all levels of business risk
Have a broad understanding of Surveillance activities and the impact an individual case or group of cases can have on product labelling
Produce and QC all required listings from Operations to ensure the needs of Surveillance and other Clinical departments are met, and attend and participate in all appropriate Surveillance meetings e.g. pre-SERM
Establish well-developed customer relationships within and outside Patient Safety
Manage the scientific and technical contribution to the maintenance of one or more of the Support Section activities within the Region
Contribute to the development and implementation of new safety-related systems, processes and procedures within the Region
Represent the Region on specific Patient Safety Process Teams
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