Compliance Principal / Compliance Analyst

Compliance Principal / Compliance Analyst

Arbetsbeskrivning

AstraZeneca (AZ) is a major international healthcare business engaged in the research, development, manufacture and marketing of prescription pharmaceuticals and the supply of healthcare services. But we're more than one of the world's leading pharmaceutical companies. At AZ, we're proud to have a unique workplace culture that inspires innovation and collaboration. Here, employees are empowered to express diverse perspectives - and are made to feel valued, energized and rewarded for their ideas and creativity.

Om tjänsten
Working with Compliance Lead in the QPPV&PV Excellence Team in Patient Safety Centre of Excellence, in Chief Medical Office (CMO), taking responsibility for the management of assigned AstraZeneca projects and partnerships including: quality and compliance monitoring, data analytics to identify root causes and continuous improvement. Accountable to develop relationships across CMO and other relevant AZ functions, to execute the delivery of the QPPV&PV Excellence continuous improvement strategy and priorities.

Dina arbetsuppgifter i huvudsak
•Drive a culture of continuous improvement, high performance, flexibility and quality emphasising a “can do” attitude and innovative approaches, across the AZ Pharmacovigilance (PV) system.
•Provides analytical support for Pharmacovigilance Compliance Systems.
•Provides expertise and resource for the design, development, implementation and continuous improvement, of a global portfolio of compliance analytics tools and reports.
•Supports the existing portfolio of reports/dashboards across various technical platforms (Spotfire, Oracle APEX, Excel VBA), further developing them and providing customer support.
•Provides analytical input where required to KPIs, internal and external benchmarks, compliance and data quality issues, as well as responding to ad hoc business requirements, including requests in support of regulatory inspections.
•Leads and/or contributes to specific projects/workstreams as required, to ensure full exploitation of compliance data.
•Acts as a key interface to customer groups and process area leads, both within and outside of Patient Safety (e.g. Operations), to understand reporting/analytical requirements and to develop technical solutions to meet those requirements.
•Provides data modelling support, specifically with a view to integrating data across Pharmacovigilance Systems
•Working with Patient Safety Process and Partnerships Leads and Patient Safety and Regulatory experts, develop, establish, monitor, report and assess global KPIs related to pharmacovigilance data reporting.
•Manage relationships/partnerships/alliances external to the CMO function that are essential to delivering AstraZeneca’s pharmacovigilance License To Operate responsibilities, e.g. with AstraZeneca affiliates.
•Working collaboratively, provide expertise and sharing best practices across all regions and in all partnerships.


Vem är du?
Education, Qualifications, Skills and Experience:
The following is highlighted:
•Technical skills in the following areas – Excel (incl. VBA), SQL, Python, visual analytics (Tibco Spotfire or similar).
•Proven competence in the development of tools and methods to exploit data in support of business decision making including data modelling, data integration (ETL).
•Proven analytical ability to interpret and integrate complex data sets and communicate them effectively.

Desired qualifications:
•Strong desire to move into a technical data/analytics role.
•Awareness of wider IS developments within AZ or the pharmaceutical industry, particularly in relation to the design and deployment of data sources, analytical tools, informatics solutions, data integration systems and practices, etc.
•Able to work independently to solve complex problems, often while working with uncertain assumptions.
•Highly developed conceptual and analytical thinking, with ability to understand multiple, complex business needs.

Desired background:
•Bachelor’s/Master’s degree or equivalent qualification in computer science or scientific discipline.
• Experience working within a regulatory environment with an understanding of regulatory processes and systems.

Om verksamheten
At AstraZeneca we work together across global boundaries to make an impact and find answers to challenges. We do this with the upmost integrity even in the most difficult situations because we are committed to doing the right thing. We continuously forge partnerships that help pursue world-class medicines in new ways, combining our people’s exceptional skills with those of people from all over the globe.

This is a consulting assignment at AstraZeneca for 6 months with possible extension +6 months, and during the period you will be employed by Poolia.
• Start Date: As soon as possible.

Please send your application on Monday 16;th of November at the latest. You are of course also very welcome to share this option with your friends.

If you have any questions or comments, please don't hesitate to contact me.

Sammanfattning

  • Arbetsplats: Poolia Väst AB
  • 1 plats
  • 6 månader eller längre
  • Heltid
  • Fast månads- vecko- eller timlön
  • Publicerat: 9 november 2020
  • Ansök senast: 16 november 2020

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