Senior Data Engineer

United States·BostonRemotesenior

OtherData EngineeringData EngineerDataHealthcareClinical Data EngineerData & AI

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Overview

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Our mission at Oura is to empower every person to own their inner potential. Our award-winning products help our global community gain a deeper knowledge of their readiness, activity, and sleep quality by using their Oura Ring and its connected app. We've helped millions of people understand and improve their health by providing daily insights and practical steps to inspire healthy lifestyles.

Empowering the world starts with living our values and empowering our team. As a quickly growing company focused on helping people live healthier and happier lives, we ensure that our team members have what they need to do their best work — both in and out of the office.

We are looking for a Senior Clinical Data Engineer to join our Research Operations team, which drives the end-to-end execution of studies that drive new feature development and validation. You’ll manage the data that forms the foundation of our clinical trials—ensuring that data pipelines are fast, transparent, and comply with all applicable regulations.

In this role, you’ll work at the frontier of R&D health sensing and gain hands-on experience with every part of the clinical database lifecycle: from design and validation through database lock and archival. Working closely with our regulatory, software, and science teams, you’ll raise the bar for how Oura runs clinical studies.

This is a remote US role with a preference for candidates based on the East coast.

We have offices in San Francisco, San Diego and Los Angeles for those who prefer hybrid or office settings. Oura employees in other major cities (like Boston and New York) occasionally gather informally at local co-working locations.

Responsibilities

~1 min read

→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

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