Senior Clinical Data Engineer
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Job Description
Senior Clinical Data Engineer overseeing clinical data lifecycle for Oura's research studies. Collaborating with teams to maintain data integrity and regulatory compliance in clinical trials.
Responsibilities:
- Oversee the clinical data lifecycle for a portfolio of studies: ensuring timelines and data integrity are maintained.
- Work closely with research project managers, algorithm developers, data engineers, and external vendors to align data management activities with broader trial objectives.
- Identify data-related risks and implement mitigation strategies, while driving process improvements and adopting emerging technologies as needed.
- Lead data quality management, query analysis, optimization, deduplication, auditing, and validation of regulated data ecosystems.
- Develop and oversee the design of Case Report Forms (CRFs) and electronic data capture (EDC) systems to ensure accurate, complete, and protocol-compliant data collection.
- Build the Clinical Data Repository that will form the backbone of all research and regulatory work at Oura
Requirements:
- 7+ years of industry experience with clinical data management
- Fluency with regulations such as ICH GCP, 21 CFR Part 11, and standards such as CDISC (SDTM/ADaM)
- Proficiency in an industry-standard EDC system (e.g. Medidata Rave, Castor, REDCap) and data engineering tools (e.g. AWS S3, Glue, Athena; Databricks; Dagster; dbt)
- Experience bridging clinical data management and research with enterprise practices and standards
- Comfort with building dashboards using tools like Tableau or Databricks
- Flexibility with scheduling to enable calls with global collaborators
Benefits:
- Competitive salary and equity packages
- Health, dental, vision insurance, and mental health resources
- An Oura Ring of your own plus employee discounts for friends & family
- 20 days of paid time off plus 13 paid holidays plus 8 days of flexible wellness time off
- Paid sick leave and parental leave
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