This position is a member of the Safety Operations team that handles country level PV activities including collection, documentation and processing of local adverse event (AE) reports from all sources.
What you will be doing
Manage collection, documentation and processing of local AE reports from all sources based on national legislations and in accordance with Baxter s procedures
Perform surveillance activities for any recent potential safety information and escalate per procedures
Perform local case triage including assessment of validity, duplicate check, and forwarding to internal and external partners as required.
Perform case intake within the Pharmacovigilance Safety System (PSS).
Respond to queries from the global case processing team.
Perform source document redaction as necessary and ensure all source documentation is captured in PSS.
Perform local quality checks as required.
Perform Health Authority case download where required
Other activities as required
What you will bring
Degree in sciences,
pharmacy or related field or minimum of 3 years pharmacovigilance experience
Excellent attention to detail
Excellent oral and written communication
Operates effectively in a team workplace
Ability to work under strict deadlines
Ability to multitask and prioritize changing workload
Medical and clinical knowledge
Ability to establish proficiency working within PSS
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