Senior Pharmacovigilance Associate
Core
Managing Individual Case Safety Reports (ICSRs) and SAE/SUSARs within a pharmacovigilance unit to ensure patient safety compliance.
Role type
Senior Pharmacovigilance Associate
Builds
Monthly safety reports and database outputs for clients
Domain
Life sciences / Pharmacovigilance
Deliverable
client delivery
Required skills
ICSR processing, SAE/SUSAR management, MedDRA and WHO coding, data reconciliation, workflow management, LCPPV/PRLS coordination
Preferred skills
None stated
Technologies
MS Office
Responsibilities
Processing ICSRs from all sources, performing ICSR follow-up, managing SAE/SUSARs (unblinding, trial reconciliation), handling product quality complaints, generating database outputs and reports, supporting PV processes, acting as LCPPV and PRLS
Seniority
Senior, hands-on IC
Sourced via smartrecruiters · Listed on CareerPlan, which tracks 70,000+ jobs from 20+ sources.
