Local Case Intake Advisor, GBS Patient Safety
About this opportunity
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
31-Jul-2026
Closing Date
13-Aug-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.
Job details
How this role compares
Computed from every other active Pharmacovigilance role in our database, not just this employer's listings.
We currently track 25 comparable Associate Pharmacovigilance roles across 14 biopharma companies.
Salary context
1 of 25 peers report a salary range (USD, annualized)
Peers share this role's job function and a matching or adjacent seniority level -- not necessarily the same therapeutic area or country.
Where these roles are based
Top locations among the 25 comparable roles
+ 6 more countries
Seniority mix
25 of 25 peers have a known seniority level
Therapeutic area mix
0 of 25 peers have a known therapeutic area; the rest are genuinely unlabeled, not hidden
No peers with a known therapeutic area yet.
Similar opportunities
The closest matches from our peer group, ranked by how similar they are, not how well you'd qualify for them -- treat this as market context, not a guaranteed shortlist; a weak match is labeled as one below.
How we calculate "similar"
No black box, no LLM guesswork: a deterministic score built from four normalized attributes. Here's this role's own peer group at different match levels, so you can see the mechanism, not just the result.
Every comparison starts from the same 100-point budget: 25 for working in the same function, 40 for the same therapeutic area, 20 for the same or adjacent seniority, 15 for the same country. A dimension we can't confirm on both sides contributes nothing, never a guess, never a free pass.
0 points, never a partial guess. A role we know almost nothing about beyond its function bottoms out at 25%; it never inflates to 100% just because there's little to compare against. Seniority uses a defined ladder (Associate → Manager → Associate Director → Senior → Principal → Director → Senior Director → Executive/VP) so "Director" and "Senior Director" count as adjacent, but "Director" and "Executive/VP" do not.