Senior Clinical Data Engineer

Oura is a company focused on empowering individuals to understand and improve their health through innovative products. The Senior Clinical Data Engineer will manage the data lifecycle for clinical trials, ensuring data integrity and compliance while collaborating with various teams to enhance clinical study processes.

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