Pharmacovigilance Associate
Core
Support the pharmacovigilance team in Israel by ensuring safety data and systems are accurate and compliant, processing safety information, and supporting reporting activities.
Role type
Pharmacovigilance Associate (Drug Safety)
Builds
Safety databases, PV records, and regulatory reports for GSK's vaccines, specialty, and general medicines portfolio.
Domain
Biopharmaceuticals / Drug Safety
Required skills
Pharmacist license (Israel), Adverse event data review and extraction, Data reconciliation, Database management, Hebrew and English communication, IT skills (Excel, web-based applications)
Preferred skills
ICSR processing, Regulatory reporting knowledge, Safety database experience (Argus, Veeva), Vendor management, Process improvement
Technologies
Argus, Veeva, Excel
Responsibilities
Review and monitor adverse event data from spontaneous and solicited sources; Perform quality checks and basic case triage; Maintain pharmacovigilance agreements and documentation; Run database listings and reports; Liaise with local teams and vendors to resolve data queries; Provide administrative support for PV processes.
Seniority
Junior to Mid-level, hands-on IC
