Clinical Data Manager
About The Position
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 Clinical Data Manager to join our Research Operations team, which drives the end-to-end execution of studies that drive new feature development and validation. In this role, you will be part of the full lifecycle of clinical study data — from database build and validation through database lock and archival — ensuring that data is compliant, traceable, and inspection-ready. You will also take a hands-on role in building data quality monitoring reports and dashboards using programming languages and analytics tools to provide real-time visibility into study health. You’ll work closely with Clinical Operations, Regulatory, Biostatistics, Science, Data Engineering, and external vendors to ensure that our data management practices meet FDA, ICH-GCP, and internal quality standards while enabling speed and scalability. 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.
Requirements
- 3+ years of industry experience in clinical data management within medical device, digital health (SaMD), biotech, or CRO environments
- Experience supporting regulated clinical trials and regulatory submissions (e.g., 510(k), De Novo, CE/MDR)
- Hands-on experience with industry-standard EDC systems (e.g., Medrio, REDCap, Rave, TrialKit)
- Strong working knowledge of ICH-GCP, 21 CFR Part 11, and data privacy regulations
- Experience managing database builds, edit checks, UAT, query resolution, and database lock activities
- Proficiency in SQL and/or Python, with demonstrated experience building data quality reports, dashboards, and validation queries
- Experience collaborating cross-functionally with Clinical Operations, Biostatistics, Regulatory, Engineering, and CRO partners
- Comfort operating in a fast-paced, product-driven environment with multiple concurrent studies
- Flexibility with scheduling to support global collaborators when needed
Nice To Haves
- Experience working with structured clinical datasets and familiarity with CDISC standards (SDTM/ADaM) preferred
Responsibilities
- Develop and maintain data quality monitoring frameworks, including defining key data quality metrics and thresholds
- Build and maintain quality dashboards and reports using programming languages (e.g., SQL, Python) and BI tools to provide near real-time study insights
- Oversee data validation, coding, reconciliation (e.g., safety, device, external vendor data), and risk-based review processes
- Ensure compliance with ICH-GCP, 21 CFR Part 11, HIPAA, and applicable FDA expectations for regulated SaMD trials
- Partner with Engineering and Data teams to support ingestion, transformation, and traceability of multi-source clinical datasets (e.g., wearable data, ePRO, device integrations, CRO exports)
- Manage CRO and vendor data management deliverables, ensuring sponsor oversight and quality standards are met
- Identify data-related risks early and drive mitigation strategies
- Contribute to SOP development and help standardize scalable, repeatable data management practices across Research Operations
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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What This Job Offers
Job Type
Full-time
Career Level
Mid Level
Education Level
No Education Listed
Number of Employees
251-500 employees
