Pharmacovigilance Specialist with English and Portuguese
Pharmacovigilance Specialist with English and Portuguese
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Salary Not Disclosed
1 Vacancy
Job Description
Home-based role
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 Portuguese.
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.
Mentor new team members and support department initiatives as assigned by the manager.
Qualifications
Bachelors degree in life sciences or a related field. (Graduated or final year)
Advanced level of English and Portuguese (mandatory will be evaluated)
1 year of previous experience in clinical research.
IQVIA is a leading global provider of clinical research services commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at
Required Experience:
Unclear Seniority
Employment Type
Full-Time
