REQ-10006523
Aug 12, 2024
Ireland

About the Role

Major accountabilities:

  • Produce analytic deliverables, including full study reports for RWE, observational database or omics data projects.
  • Independently draft and edit documents such as high level research proposals, protocols and statistical analysis plans.
  • Conduct observational data analyses involving new creative approaches and oversee data management and statistical programming activities.
  • Provide guidance to conduct data quality reviews with detailed documentation.
  • Present research and analysis results to customers and stakeholders.
  • Produce analysis datasets, listings, tables, and figures for research projects, according to specifications, while maintaining documentation and complying with pre-defined project / study standards.
  • Perform in-depth research and quantitative and qualitative analysis independently. Provide guidance to Associate RWE Research Analysts and RWE Research Analysts.
  • Develop department-level standards, tools and templates.
  • Collaborate with Evidence and Launch Excellence (ELE) to drive quality and accuracy of deliverables; constant improvements on systems, processes and quality matrices that add value to existing solutions.
  • Help on-board new team members, as appropriate, and complete special projects as assigned.
  • Regularly elicit customers' satisfaction levels. Identify service areas requiring attention.

Minimum requirements:

  • Experience in the application of statistical methods to the analysis of observational data.
  • Technical proficiency in analytical and visualization tools and statistical programming languages such as SAS, R, R/shiny, Tableau, Spotfire, SPSS, STATA, WinBUGs.
  • Deep knowledge of RWE data sources and standards such as MarketScan, CPRD, JMDC, Optum, PharMetrics, OMOP.
  • Expert in applied statistics. Extensive experience in the application of statistical methods for analysis of observational data including propensity scores, sensitivity analyses, etc. is a plus.

Preferred Qualifications:

  • Postgraduate qualification (Masters or PhD) in bioinformatics.
  • Publications or presentations in recognized RWE/biomedical journals/conferences highly desired.
  • Prior experience working in pharma/biotech/CRO/RWE organizations.

Role Requirements

Why Novartis: Helping people with disease and their families takes more than innovative science. It takes a community of smart, passionate people like you. Collaborating, supporting and inspiring each other. Combining to achieve breakthroughs that change patients’ lives. Ready to create a brighter future together? https://www.novartis.com/about/strategy/people-and-culture

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Benefits and Rewards: Read our handbook to learn about all the ways we’ll help you thrive personally and professionally: https://www.novartis.com/careers/benefits-rewards

Operations
CTS
Ireland
Dublin (NOCC)
Market Access
Full time
Regular
No
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REQ-10006523

Real World Evidence Research Analyst

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