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.
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 (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)
What we offer to you
- OSDE 310
- Annual bonus by performance
- Salary adjustments during the year according to inflation rates.
- 21 vacations days
- Work flexibility
- 100% remote role