Buenos Aires, ArgentinaFull timeR
Job Overview
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!
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