Pharmacovigilance Associate

GSK remains committed to achieving bold commercial ambitions for the future. By 2031, we aim to deliver £40 billion in annual sales, leveraging our existing strong performance momentum to significantly increase our positive impact on the health of billions of patients globally. Our Ahead Together strategy is centred on early intervention to prevent and alter the course of disease, thereby protecting people and supporting healthcare systems. Our diverse portfolio consists of vaccines, specialty medicines, and general medicines. Through continuous innovation and a dedicated focus on scientific and technical excellence, we strive to develop and launch new, groundbreaking treatments that address critical health challenges.

Position Summary

You will support the pharmacovigilance (PV) team in Israel by ensuring safety data and related systems are accurate and compliant. You will work closely with global and local colleagues, vendors and partners to process safety information, maintain PV records, and support reporting activities. We value accuracy, clear communication and a collaborative mindset. This role offers growth, meaningful impact on patient safety, and alignment with GSK's mission of uniting science, technology and talent to get ahead of disease together.

Responsibilities

This role will provide YOU the opportunity to lead key activities to progress YOUR career. These responsibilities include some of the following:

• 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.

Why You? Basic Qualifications & Skills

• Pharmacist with Israeli license.
• 1-4 years' experience in pharmacovigilance / drug safety.
• Strong attention to detail and experience with data entry, reconciliation or database work.
• Good IT skills, including Excel and experience with web-based applications or safety databases.
• Ability to communicate clearly in Hebrew and English, both written and verbal.
• Comfortable working in a matrixed team and responding to stakeholders in a timely way.

Preferred Qualifications & Skills

• Experience with ICSR (Individual Case Safety Report) processing.
• Knowledge of local regulatory reporting requirements and pharmacovigilance methodology.
• Prior experience with safety databases (e.g., Argus, Veeva or similar) or document management systems.
• Experience working with vendors or in quality and compliance activities.
• Demonstrated experience in process improvement or KPI analysis.

Working arrangements

This role is hybrid. You will be expected to work on-site in Israel regularly and have flexibility for remote working as agreed with your manager.

How to apply

If this role matches your skills and ambitions, we encourage you to apply. Tell us how your experience fits the responsibilities and qualifications. We look forward to hearing how you can contribute to patient safety and grow with our team.