Pharmacovigilance Specialist
Core
Review, assess, and process safety data and information across service lines, including collecting and tracking incoming Adverse Events (AEs), database entry, coding, and writing narratives.
Role type
Pharmacovigilance Specialist
Builds
Safety reports and data distributions for internal and external third parties
Domain
Life sciences / Healthcare / Pharmacovigilance
Deliverable
production ML models | product features | dashboards & analysis | research | client delivery | infrastructure | physical/clinical work
Required skills
Adverse Event (AE) tracking, database entry, AE coding, narrative writing, literature review, SOP compliance, regulatory compliance
Preferred skills
Clinical experience, pharmacovigilance experience
Technologies
Safety databases, coding systems
Responsibilities
Process safety data according to regulations and SOPs, perform pharmacovigilance activities including AE tracking and coding, ensure compliance with quality and delivery standards, liaise with functional team members and healthcare professionals
Seniority
Entry to Mid-level, hands-on IC
