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AstraZeneca

Local Case Intake Advisor, GBS Patient Safety

AstraZeneca is hiring a Local Case Intake Advisor, GBS Patient Safety in Lisbon, Portugal. Level rates it ; you can apply on AstraZeneca.

Level's read on this job

  • On Level's scale, this role is Little AI ●○○○: aI is not part of the work.
  • The posting mentions Argus, pharmacovigilance and safety reporting among its tools and skills.
  • Level classes it as a mid-level role.
  • AstraZeneca has 1,300+ other open roles on Level.

AI in this role

Manage adverse event reports and process safety cases to ensure compliance with pharmacovigilance regulations.

Argus
pharmacovigilancesafety-reportingregulatory-compliancepharmacymedical-case-processing
Local Case Intake Advisor – GBS Patient Safety - Hungarian Speaker

📍 Portugal (supporting Hungary) - 1 Year Fixed Term Contract

Bring your expertise. Shape patient safety. Transform lives.

At AstraZeneca, every role plays a part in improving patient outcomes worldwide. As a Local Case Intake Advisor within our Global Business Services (GBS) Patient Safety team, you’ll help ensure the highest standards of pharmacovigilance, protecting patients and supporting the safe use of our medicines.

This is a fantastic opportunity to work at the intersection of science, compliance, and collaboration in a fast-paced, global environment.

About the role:

As a Local Case Intake Advisor, you will manage the intake and processing of Individual Case Safety Reports (ICSRs) at a local level, supporting designated AstraZeneca Marketing Companies.

Acting as a key liaison between local teams and Global Patient Safety, you’ll ensure compliance with internal procedures and external regulatory requirements while delivering high-quality pharmacovigilance operations.

What you’ll do:

  • Manage and process adverse event reports and ICSRs 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
  • Identify and manage product quality complaints (PQC) and related safety reporting
  • Perform reconciliations to ensure accuracy of pharmacovigilance data
  • Conduct literature searches and regulatory database screening where required
  • Collaborate closely with local Patient Safety teams and cross-functional stakeholders
  • Provide expertise and guidance to resolve local case intake issues

Essential skills & experience:

  • Degree in Pharmacy, Medicine, or Life Sciences
  • Knowledge of pharmacovigilance (PV) and health authority regulations
  • Strong attention to detail and analytical mindset
  • Excellent written and verbal communication skills
  • Ability to work collaboratively across functions and geographies
  • Problem-solving skills with the ability to manage moderate complexity

Desirable:

  • Experience in audits and inspections
  • Knowledge of AstraZeneca therapeutic areas
  • Project management experience
  • Familiarity with safety systems (e.g. Argus)
  • Additional language skills

Languages:

Fluency in:

  • English (Essential)
  • Hungarian (Essential)

Why AstraZeneca?

At AstraZeneca, you’ll be empowered to make a difference in a company driven by science and patient impact. We foster a collaborative, inclusive environment where innovation thrives and your development is supported every step of the way.

  • Work in a global, purpose-driven organisation
  • Be part of a high-performing Patient Safety function
  • Access to continuous learning and career development opportunities
  • Contribute to improving the lives of millions of patients worldwide

Ready to make an impact?

Apply now and help us deliver life-changing medicines with the highest standards of safety and care.

Date Posted

19-paź-2026

Closing Date

08-lis-2026

AstraZeneca embraces diversity and equality of opportunity. We are committed to building an inclusive and diverse team representing all backgrounds, with as wide a range of perspectives as possible, and harnessing industry-leading skills. We believe that the more inclusive we are, the better our work will be. We welcome and consider applications to join our team from all qualified candidates, regardless of their characteristics. We comply with all applicable laws and regulations on non-discrimination in employment (and recruitment), as well as work authorization and employment eligibility verification requirements.

How we rate this

Local Case Intake Advisor, GBS Patient Safety at AstraZeneca rates 0 out of 100 for how much of the daily work is AI. That makes it Little AI (AI Level 1 of 4). The level is about AI in the job, not seniority.

Classification

Little AI. AI is not part of the work.

  1. ●●●● Builds AI80 to 100
  2. ●●●○ Works on AI60 to 79
  3. ●●○○ Uses AI40 to 59
  4. ●○○○ Little AI0 to 39

Levels come from how often the tools, models and workflows of the role are named in the posting itself. Read the description and count the AI tools, models and workflows it names.

Prepare for this job

Built from this posting and from similar jobs on Level.

Skills and AI tools this role asks for

PharmacovigilanceSafety ReportingRegulatory CompliancePharmacyMedical Case ProcessingArgus

Questions you could be asked

  1. Tell me about a project where pharmacovigilance was part of your work. What did you do?
  2. Tell me about a project where safety reporting was part of your work. What did you do?
  3. Tell me about a project where regulatory compliance was part of your work. What did you do?
  4. Tell me about a project where pharmacy was part of your work. What did you do?
  5. Tell me about a project where medical case processing was part of your work. What did you do?

Adapt your resume

  • List these exact terms on your resume: Pharmacovigilance, Safety Reporting, Regulatory Compliance, Pharmacy, and Medical Case Processing. An applicant tracking system matches the wording, not the idea.
  • Attach one line of real, concrete experience to at least one of them. A tool named with nothing behind it rarely survives a human read.

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