Pharmacovigilance (PV) Associate – Israel

About the role

GSK is seeking a Pharmacovigilance (PV) Associate to support its safety operations in Israel. You will ensure that adverse event data are accurately captured, processed and reported in compliance with local and global regulations, contributing to patient safety and the company’s mission.

Key responsibilities

• Review, extract and monitor adverse event data from spontaneous and solicited sources in safety databases.
• Perform quality checks, reconciliations and basic case triage to ensure data completeness and timeliness.
• Maintain pharmacovigilance agreements, safety documentation and document repositories.
• Generate database listings, reports and support metric collection and trend analysis.
• Liaise with local operating companies, vendors and internal teams to resolve data queries.
• Provide administrative and system support for PV processes, including mailbox triage and document archiving.

Required profile

• Pharmacist with a valid Israeli license.
• 1–4 years of experience in pharmacovigilance or drug safety.
• Strong attention to detail and experience with data entry and reconciliation.
• Excellent written and verbal communication in Hebrew and English.
• Ability to work effectively in a matrixed, cross‑functional environment.

Required skills

• Proficiency in Microsoft Excel.
• Experience with web‑based applications and safety databases (e.g., Argus, Veeva).

What we offer

• Opportunities for professional growth within a global pharmaceutical leader.
• Direct impact on patient safety through robust pharmacovigilance activities.
• Collaborative and supportive work environment aligned with GSK’s “Ahead Together” strategy.