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Associate Director, Global Patient Safety

Ort Warschau, Woiwodschaft Masowien, Polen Anzeigen-ID R-220281 Veröffentlichungsdatum 20/02/2025

Location: Warsaw, Poland
Hybrid model of work: 3 days in office, 2 remote per week

At AstraZeneca, we pride ourselves on crafting a collaborative culture that champions knowledge-sharing, ambitious thinking and innovation – ultimately providing employees with the opportunity to work across teams, functions and even the globe.


Recognizing the importance of individualized flexibility, our ways of working allow employees to balance personal and work commitments while ensuring we continue to create a strong culture of collaboration and teamwork by engaging face-to-face in our offices 3 days a week. Our office in Warsaw is purposely designed with collaboration in mind, providing space where teams can come together to strategize, brainstorm and connect on key projects.

Our dedication to sustainability is also central to our culture and part of what makes AstraZeneca a great place to work. We know the health of people, the planet and our business are interconnected which is why we’re taking ambitious action to tackle some of the biggest challenges of our time, from climate change to access to healthcare and disease prevention.

The role holder is accountable for the effective delivery (on time and budget) of Patient Safety solutions and services to the GPS Cross-TA functions to underpin the delivery of clinical projects to meet the Global Patient Safety Therapeutic Areas (GPS TAs) partner expectations. The GPS Cross TAs include Global Markets, Operations, Technology & Analytics, Patient Safety Risk Management, QPPV and PhV Excellence, Cardiovascular Safety and Specialist Knowledge Groups. The role holder contributes to the effective strategy of the GPS team through liaison and discussion with BPO, procurement, Alliance Management and GPS Executive / Senior Directors. The Associate Director, GPS will use enterprise knowledge and specific  Patient Safety  knowledge to deliver high standards, with a growing freedom to act without direct supervision. The impact is directly related to the quality of licence to operate solutions developed, the service provided and the degree of influence the role has on others.

Typical Accountabilities

  • Supports the overall improvement of enabling activities relating to GPS including owning the clinical safety strategy, post-marketing signal surveillance, automation and innovation; including troubleshooting problems & developing solutions.
  • Drives the annual PV Net data collection and submission, identifying PV resources across the GPS team.
  • Acts as the interface between AZ and Alexion procurement, to support Alliance Management contracts and able to provide context on Alexion safety cost drivers.
  • Acts as the interface between AZ Portfolio & Capacity Management to understand Alexion systems and algorithms.
  • Tracks Alexion funded roles and incumbents.
  • Supports the planning, execution and tracking of external interactions/publications to demonstrate the impact of GPS.
  • Provides specialist project based support when required.
  • Periodic Safety Report scheduling/maintenance.
  • Responsible for Patient Safety Document Management (PSDM) support, training, and QC (monthly and quarterly).
  • Development of dashboards and analytics to support GP delivery.
  • Supports the smooth running of specialist GPS committees and processes, offering advice and prioritising schedules i.e., such as Safety Information Review Committee (SIRC), Specialist Knowledge Groups (SKGs)
  • Develops and maintains relevant information assets such as SharePoint site, and tools used by GPS in ways that enable effective sharing, re-use, accessibility, and quality to support above deliverables.
  • Responsible for enterprise wide Revalidation for UK GMC registered Physicians.

Education, Qualifications, Skills and Experience

  • Understanding of Patient Safety and/or Pharmacovigilance Area including its compliance requirements
  • 5+ years Biopharmaceutical Experience
  • BA degree or equivalent in scientific field of study
  • Pharmaceutical/Clinical strategy development experience
  • Mastery in use of Microsoft Office products
  • Experience in working Cross Functionally
  • Proven track record in working and influencing across cultures and different geographical regions
  • Good attention to detail
  • Organizational skills in planning and driving initiatives with tight timelines
  • High level of comfort with learning new technologies and applying them to make work more efficient

Are you interested in working at AZ, apply today!

AstraZeneca is an equal opportunity employer that is committed to diversity and inclusion and providing a workplace that is free from discrimination. AstraZeneca is committed to accommodating persons with disabilities.



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