Pharmacovigilance Specialist
hace 3 semanas
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 French.
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
- Bachelor's degree in life sciences or a related field.
- Up to 3 years of relevant experience, including up to 1 year of pharmacovigilance experience.
- Fluency in English, Spanish, and French.
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