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Job description

Do you have experience from working within a regulatory environment and strong technical skills in Excel, SQL, Python and visual analytics? We now have an exciting opportunity to join AstraZeneca for a 6 month consultancy assignment.

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.

Responsibilities

  • 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.

Qualifications

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
For us, it is important that all competence and skills in the labor market are utilized. We welcome all applicants and strive for diversity.

Application

2020-11-17, selection and interviews will be ongoing. The position may be filled before the last day of application, therefore, apply as soon as possible.

For more information: Birgitta Nyström, [email protected]

About the company

Randstad Life Sciences is specialized in competences within Life Science. As a consultant with us, you get a competitive salary, benefits and collective agreements. Your consultant manager is always there for you and ensures that you get varying and developing assignments at different companies, within different industries. At Randstad Life Sciences, your personal development is in focus, and you are offered a large network and many social activities.

Randstad Life Sciences is part of Randstad, the world leader in recruitment and consulting with operations in 38 countries. With this global network, in combination with our strong local foundation, we can offer a wide range of varied and developing assignments and jobs for you who are a specialist in life science. Our mission is to help you reach your true potential with your career in focus!

Detta är en jobbannons med titeln "Compliance Analyst, AstraZeneca Gothenburg" hos företaget Randstad AB och publicerades på webbjobb.io den 9 november 2020 klockan 17:30.

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