LS EU Domain SME


  • Lead Life Sciences consulting proposals and delivery efforts including developing the project logic, project design, detailed work streams, team structure, and deliverables
  • Develop strong key client relationships, managing client expectations and presenting final recommendations persuasively to senior teams
  • Develop a strategic vision around enterprise data management while guiding the client around regulatory requirements
  • Facilitate and lead working sessions with clients, subject matter experts, stakeholders, consulting teams and technical teams
  • Help our clients assess their current digital technology maturity, identify gaps and shape a comprehensive, end-to-end digital blueprint and technology roadmap
  • Isolate key client issues as part of a pursuit or delivery effort and identify potential solutions to address those issues through a consultative approach
  • Partner with other Practices and Delivery teams to ensure success in pursuits and delivery
  • Develops governance process and criteria for evaluating and managing projects
  • Play a key role as a visible leader throughout the enterprise leading change and delivering value


    Bachelor’s degree required; Masters in a relevant field from a top university preferred or equivalent level of evidence of business understanding through work experience.


• Proven thought leadership in the Life Science industry with a background in enterprise data management, data science involvement and data governance

  • 10+ years Pharma/Life Sciences or Medical Device industry experience with strong knowledge of the EU markets and environment
  • 10+ years in Domain Consulting and Information Architecture with experience in at least one master data management project
  • Strong stakeholder management and interpersonal skills
  • Structured thinker; ability to present complex concepts in concise terms across all levels of the organisation
  • Good understanding of a range of analysis, visualisation and modelling techniques
  • Good understanding of the regulatory environment including HIPAA, GxP and GDPR
  • Strong knowledge of Medidata Rave and other trial management systems, CDISC standards
  • Working knowledge of FIHR and HL7 standards, EMR data, Safety Data and integration methods
  • Ability to lead teams across multiple functions / geographies
  • Comfortable designing and facilitating workshops involving a broad spectrum of stakeholders
  • Nice to have – working knowledge on AI and ML models leveraging large data lakes
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