Pharmacovigilance Associate

About the role

GSK is looking for a Pharmacovigilance Associate to join its PV team in Israel. You will support the team in keeping safety data and related systems accurate and compliant, working closely with global and local colleagues, vendors and partners to process safety information, maintain PV records and support reporting. The role is hybrid, with regular on-site presence in Israel and flexibility for remote work as agreed with your manager.

Key responsibilities

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

Required profile

• Pharmacist with an Israeli license.
• 1-4 years' experience in pharmacovigilance or drug safety.
• Ability to communicate clearly in Hebrew and English, written and verbal.
• Comfortable working in a matrixed team and responding to stakeholders in a timely way.

Required skills

• Strong attention to detail and experience with data entry, reconciliation or database work.
• Good IT skills, including Excel and web-based applications or safety databases.
• Preferred: ICSR processing, knowledge of local regulatory reporting requirements, experience with safety databases (e.g. Argus, Veeva) or document management systems, vendor or quality/compliance experience, and process improvement or KPI analysis experience.