This is what you will do

Process owner (cross-functional) for developing a wide range of pharmacovigilance documents for the assigned global products within the specific therapeutic area, including but not limited to Periodic Safety Reports, Safety Strategy and Core Benefit-Risk Documents.

You will be responsible for

Aggregates (PBRERs/PSURs, PADERs, RMPs, DSURs, ACOs)

•    To support the Coordinator in the global planning (for both molecules under development and those with a Marketing Authorisation);

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