Pharmacovigilance Specialist (Fluent in English + Italian)

Review, assess, and process safety data and information across service lines, received from various sources. Distribute reports/data to both internal and external third parties following applicable regulations, Standard Operating Procedures (SOPs), and internal guidelines under the guidance and support of senior operation team members. This is a trilingual role requiring fluency in English, Spanish, and Italian.

• →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.
   

• 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)