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1–2 jobs· newest first

Local Case Intake Advisor, GBS Patient Safety - French Language (9 month FTC)New
AstraZeneca · Lisboa, Portugal
Contract
Local Case Intake Advisor, GBS Patient Safety - French Language (9 month FTC)New
AstraZeneca · Lisbon, Portugal
Contract

+10K new in the last hour

Local Case Intake Advisor, GBS Patient Safety - French Language (9 month FTC)

AstraZeneca · Posted Nov 11, 2026

Lisboa, Portugal
Contract

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Manage the intake and processing of Individual Case Safety Reports (ICSRs) at a local level for AstraZeneca Marketing Companies, ensuring compliance with regulatory requirements and supporting global patient safety operations.

Responsibilities

Manage and process adverse event reports and ICSSRs from post-marketed sources
Support Health Authority interactions and queries related to safety cases
Review, assess, and distribute safety data in line with regulatory requirements and SOPs
Contribute to Quality Management Systems, including audit readiness and compliance activities
Support pharmacovigilance activities across organised data collection programs, digital channels, and partnerships

Requirements

Degree in Pharmacy, Medicine, or Life Sciences
Nice to have: audits
Nice to have: inspections
Nice to have: knowledge of AstraZeneca therapeutic areas
Nice to have: project management

Skills

pharmacovigilance health authority regulations attention to detail analytical mindset written communication verbal communication collaboration problem solving moderate complexity management Argus

See full job description

Local Case Intake Advisor, GBS Patient Safety - French Language (9 month FTC)

AstraZeneca · Posted Nov 11, 2026

Lisbon, Lisbon District, Portugal
Contract

Apply with RefersoAI Apply on careers page

Manage the intake and processing of Individual Case Safety Reports (ICSRs) at a local level, supporting designated AstraZeneca Marketing Companies.

Responsibilities

Manage and process adverse event reports and ICSSRs from post-marketed sources
Support Health Authority interactions and queries related to safety cases
Review, assess, and distribute safety data in line with regulatory requirements and SOPs
Contribute to Quality Management Systems, including audit readiness and compliance activities
Support pharmacovigilance activities across organised data collection programs, digital channels, and partnerships

Requirements

Degree in Pharmacy, Medicine, or Life Sciences
Nice to have: audits
Nice to have: inspections
Nice to have: knowledge of AstraZeneca therapeutic areas
Nice to have: project management

Skills

pharmacovigilance health authority regulations attention to detail analytical mindset written communication

verbal communication

problem solving

moderate complexity management

See full job description