You will work closely with global and local colleagues, vendors and partners to process safety information, maintain PV records, and support reporting activities.

The role involves:

• Reviewing, extracting and accurately monitoring adverse event (AE) data from spontaneous and solicited sources in safety databases according to procedures.
• Performing quality checks, reconciliations and basic case triage to ensure data completeness and timeliness.
• Maintaining and updating pharmacovigilance agreements, safety documentation and document repositories.
• Running database listings and reports; supporting metric collection and basic trend checks.
• Liaising with local operating companies, vendors and internal teams to gather information and resolve data queries.
• Providing administrative and system support for PV processes, including mailbox triage and document archiving.

Requirements:

• 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:

• 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.

This role is hybrid, requiring regular on-site work in Israel with flexibility for remote working as agreed with your manager.

Job Data by YubHub.