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Qureight

Senior Clinical Data Engineer

Qureight

. Prepare clinical trial data from sponsors and CROs to each study’s data transfer specification .

Posted 10/17/2026full-timeCambridge • United KingdomSeniorWebsite

Core Competencies

Role fit
Core Competencies

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Demonstrates expertise in building and maintaining production data pipelines, implementing CDISC standards, and collaborating with data scientists in a regulated GxP environment. Proficient in Python and familiar with machine learning workflows, ensuring data quality and reproducibility.

Highest-signal resume keywords
CDISC StandardsPython ProgrammingData Pipeline DevelopmentWorkflow Orchestration ToolsClinical Trial Data Management

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills
Data ValidationMachine Learning PreparationStatistical ModellingAutomated TestingData VersioningFeature Table CreationData Transfer SpecificationReproducible EnvironmentsData Quality ChecksClinical Data Structures
Soft Skills
CollaborationCommunicationCuriosity
Tools & Technologies
DagsterAWSDockerKubernetesDVCMLflowPandasNumPyPanderaPytest
Industry Keywords
GxPISO 13485Clinical TrialsRespiratory Disease TrialsInterstitial Lung Disease TrialsMedical Imaging DataDICOM Format

Tech Stack

Tools & technologies
AWSCloudDockerKubernetesNumpyPandasPython

About the role

Key responsibilities & impact
  • Prepare clinical trial data from sponsors and CROs to each study’s data transfer specification
  • Build analysis-ready datasets for modelling and machine learning, including ADaM-style datasets where required
  • Design, build and maintain reproducible pipelines combining imaging biomarkers and clinical data
  • Build on existing Dagster study pipelines, analytics workflow libraries and the Qureight platform
  • Build and test pipelines against dummy or interim data before database lock
  • Deliver CDISC formats, including SDTM and ADaM, where required
  • Work with Data Scientists to understand analytical workflows and automate repetitive steps
  • Implement versioned data, code and environments, with lineage and validation checks
  • Develop shared tooling, templates and libraries for standardised analysis workflows
  • Help Data Scientists move code from notebooks into tested workflows
  • Support traceability and change control expected in a regulated GxP environment
  • Collaborate with Qureight’s Data Engineering team and share standards, best practices and ideas

Requirements

What you’ll need
  • Proven experience as a Data Engineer or clinical data programmer, ideally working closely with data scientists, analysts or researchers
  • Hands-on experience with CDISC standards, particularly SDTM and ADaM, on clinical trial data
  • Experience handling clinical trial data from sponsors or CROs, including data transfers, EDC extracts, visit structures and database lock
  • Strong Python skills gained in a commercial setting, including pandas, NumPy, pandera and pytest
  • Experience building and maintaining production data pipelines with automated testing and CI/CD
  • Experience implementing data validation and quality checks
  • Experience with workflow orchestration tools such as Dagster and cloud infrastructure on AWS
  • Good working understanding of data science workflows, including statistical modelling and machine learning
  • Understanding of clinical trial data structures and uses, including endpoints, visit schedules and missing data
  • Strong collaboration and communication skills, with a service-minded collaborative approach
  • Curiosity to understand where data comes from and how it will be used
  • Experience with data versioning and experiment tracking tools such as DVC, MLflow or Dagster asset lineage
  • Experience preparing data for machine learning and longitudinal modelling, including feature tables and leakage-avoiding train/test splits
  • Experience with containerisation and reproducible environments such as Docker and Kubernetes
  • Experience with medical imaging data such as CT or MRI in DICOM format or clinical trial data
  • Experience working in regulated, GxP or ISO 13485 environments
  • Experience in respiratory or interstitial lung disease trials

Benefits

Comp & perks
  • Annual bonus plan
  • Private medical insurance
  • Life insurance
  • Cycle-to-work scheme
  • Contributory pension scheme
  • Equity
  • 28 days’ holiday allowance
  • 25 days’ annual leave
  • 3 additional company days between Christmas and New Year
  • Bank holidays
  • Enhanced family leave
  • Diverse work environment with multidisciplinary expertise