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Clinical Data Engineer II​/III

Job in San Mateo, San Mateo County, California, 94409, USA
Listing for: ClearNote Health
Full Time position
Listed on 2026-08-31
Job specializations:
  • IT/Tech
    Data Engineering, Data Warehousing, Data Analyst
Salary/Wage Range or Industry Benchmark: 150000 - 190000 USD Yearly USD 150000.00 190000.00 YEAR
Job Description & How to Apply Below

Clear Note Health is an early cancer detection company focused on the development and commercialization of non-invasive epigenomic tests to detect cancer through a standard blood draw, earlier than existing methods and when the disease is still treatable. Leveraging its novel liquid biopsy technology, Clear Note Health is initially focused on high-mortality cancers with the greatest need for early detection, starting with pancreatic and ovarian cancers.

Position

Summary

The Clinical Data  Engineer II/IIIownsclinical Data Operations:thedatapipelines, data warehouse, and reporting infrastructure that transformclinical data,laboratorydata,and sequencing results into validated, audit-ready clinical and business data. Thispositionoperatesina regulated environment in which accuracy and traceability are as important as well-architected code. The role combines hands-on pipeline and data-modeling work with ongoing production data support for our clinical studyoperations andis central to the integrity of the data that informs our research and clinical decisions.

Key Responsibilities
  • Build andmaintainELT pipelines from clinical source systems — and non-standard sources such as ad hoc spreadsheets — into ourdata warehouse, and design ingestion frameworks that adapt to evolving report formats
  • Support bulk data transfer initiatives to external partners and client-facing destinations, including the definition of the data contracts those partners depend on
  • Develop, test, and refactor data transformation models across core clinical schemas, implementing precise, well-specified business logic, and integrate clinical data with other corporate data
  • Define methods and metrics for assessing data quality, and monitor andmaintaindata quality across clinical datasets
  • Own the reliability of clinical result data end to end, tracing issues to their root cause and strengthening controls through documented change management
  • Strengthen the resilience of data contracts and design reconciliation logic that unifies data from multiple sources into a single, authoritative record
  • Serve as a trusted partner to clinical and laboratory operations and external stakeholders, resolving data questions and improving accuracy at the source
  • Build andmaintaindashboards and monitoring, including those subject to formal system validation, and support the data needs of adjacent business systems
  • Partner with the Regulatory/QA team to ensure clinical data flow and the data warehouse remain compliant with procedural and regulatory requirements
  • Serve as a subject-matter expert on warehouse clinical data, providing technical guidance and training to research and development teams
  • Provide project status updates to cross-functional stakeholders
Qualifications
  • 5+ years of hands-on data engineering experience with production data-transformation frameworks (dbtpreferred) and a cloud data warehouse
  • Software-engineering fundamentals and an expert understanding of database and data-warehouse concepts
  • Deep SQL expertise, including the ability toidentifysubtle logic errors in complex queries
  • Experience with ELT and data-integration tools
  • Experience with designing,buildingandusingcontainers
  • Proficiency in Python or a comparable scripting language
  • Familiarity with cloud identity and access-management concepts (key-pair authentication, OAuth/OIDC, workload identity federation)
  • Proven ability to work in a regulated environment, including precise documentation, change-control processes, and audit trails
  • Enjoys a role that balances building new data systems with keeping production systems reliable and trusted
  • Strong written and verbal communication skills, witha track recordof documenting your work
  • Working knowledge of clinical or laboratory data systems is a plus
  • Familiarity with clinical data standards (CDASH/CDISC) preferred
  • Working knowledge of Good Clinical Practice (GCP) and the clinical trial process preferred
  • Familiarity with cancer-related medical classifications and ontologies (e.g., ICD-10) a plus

On-site is preferred for this position, in either our San Diego or San Mateo office. Theanticipatedsalary range for this position is $150,000 - $190,000. The actual salary will be…

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