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

Main Responsibilities

• 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.
  

Qualifications

• Bachelor’s degree in Life sciences or a related field

• Fluency in English and Italian, C1 level minimum. Mandatory and will be evaluated.

• Up to 3 years of previous clinical experience (desirable)

• 1 year of pharmacovigilance experience will be highly valued (desirable)

Work modality: 100% home-based

Full-time role, Monday to Friday

Will require to work on national ARG holidays