Remote Pharmacovigilance Specialist (EN/ES/IT)
IQVIA
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Benefits dieser Stelle
Zusammenfassung
IQVIA is seeking a safety data reviewer to process and assess pharmacovigilance information across service lines, ensuring regulatory compliance and timely data delivery under senior guidance.
The role is trilingual (English, Spanish, Italian) and remote (100%); requires a Life sciences degree, English and Italian fluency, and up to 3 years of clinical/pharmacovigilance experience.
IQVIA offers performance bonuses, inflation adjustments, generous vacation, flexible work, and a fully remote setup.
Qualifikationen
- Bachelor’s degree in Life sciences or a related field (mandatory)
- Fluency in English and Italian (mandatory) (will be evaluated)
- Up to 3 years of previous clinical experience (desirable)
- 1 year of pharmacovigilance experience will be highly valued (desirable)
Aufgaben
- Process safety data according to applicable regulations, guidelines, SOPs, and project requirements.
- Perform pharmacovigilance activities, including collecting and tracking incoming Adverse Events (AEs) and endpoint information, determining initial/update status of incoming events, database entry, coding AEs and products, writing narratives, and literature-related activities.
- Ensure compliance with quality, productivity, and delivery standards per project requirements.
- Liaise with different functional team members and healthcare professionals to address project-related issues.
Kenntnisse
Ausbildung
Jobbeschreibung
IQVIA is seeking a safety data reviewer to process and assess pharmacovigilance information across service lines, ensuring regulatory compliance and timely data delivery under senior guidance.
The role is trilingual (English, Spanish, Italian) and remote (100%); requires a Life sciences degree, English and Italian fluency, and up to 3 years of clinical/pharmacovigilance experience.
IQVIA offers performance bonuses, inflation adjustments, generous vacation, flexible work, and a fully remote setup.
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