Collect, assess and process adverse event information (clinical and post marketing) in a compliant and timely manner in order to comply with global regulations which includes:Seriousness assessmentLabelingCausalityInitial and Follow - upMeeting company standards for quality, compliance and productivity.Remaining current on knowledge and skills required for case processing.Skills/Qualifications Pharmacovigilance experienceAegis database experienceAttention to detailWork well within a teamDisplay positive attitudeBachelor’s degree with related health sciences background, RN, BSN, BS, BS Pharm.
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