Pharmacovigilance Intake Specialist
$112,000–$112,000 year
On-siteWarsaw, Mazovia, Poland
Job Summary
Manage collection, documentation, and processing of local adverse event reports from all sources in accordance with national legislations and Baxter procedures. Perform surveillance activities for new potential safety information, conduct local case triage including validity assessment and duplicate checks, and forward cases to internal and external partners as required. Perform case intake within the Pharmacovigilance Safety System, respond to queries from the global case processing team, execute source document redaction, and perform local quality checks. Handle Health Authority case downloads where necessary. This role is part of the Safety Operations team dedicated to country-level PV activities.
Required Qualifications
- Excellent attention to detail
- Excellent oral and written communication
- Operates effectively in a team environment
- Ability to work under strict deadlines
- Ability to multitask and prioritize changing workload
- Medical and clinical knowledge
- Ability to establish proficiency working within PV database
- Degree in sciences, pharmacy or related field or minimum of 3 years pharmacovigilance experience
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