- Страна
- США
- Зарплата
- 147 900 $ – 203 000 $
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Senior Clinical Data Engineer
Oura — лидер рынка носимых устройств с сильной инженерной культурой. Вакансия предлагает конкурентную зарплату, опционы и возможность работать над продуктом, реально улучшающим здоровье людей.
Сложность вакансии
Роль требует редкого сочетания глубоких знаний в области клинических исследований (GCP, CDISC) и современных навыков дата-инжиниринга (AWS, Databricks, dbt). Высокий порог входа обусловлен необходимостью работать в строго регулируемой среде.
Анализ зарплаты
Предлагаемая зарплата ($147k - $203k) полностью соответствует и даже местами превышает рыночные ожидания для Senior Data Engineer в США, особенно учитывая узкую специализацию в Clinical Data.
Сопроводительное письмо
I am writing to express my strong interest in the Senior Clinical Data Engineer position at Oura. With over seven years of experience in clinical data management and a deep understanding of ICH GCP and 21 CFR Part 11 regulations, I am excited about the opportunity to contribute to your Research Operations team. My background in bridging the gap between clinical data standards like CDISC and modern data engineering tools such as AWS, Databricks, and dbt aligns perfectly with Oura's mission to innovate in the health-sensing space.
In my previous roles, I have successfully overseen the entire clinical database lifecycle, from CRF design in EDC systems like Medidata Rave to the final database lock. I am particularly drawn to Oura's commitment to data integrity and transparency in clinical trials. I am confident that my technical proficiency in building robust data repositories and my experience in mitigating data-related risks will help raise the bar for how Oura executes its clinical studies and validates new features.
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Описание вакансии
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.
What You’ll Do:
- 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
We would love to have you on our team if you have:
- 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
At Oura, we care about you and your well-being. Everyone here at Oura has a ring of their own and we are continually looking to improve employee health.
What we offer:
- 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
Oura takes a market-based approach to pay, which may vary depending on your location. US locations are categorized into tiers based on a cost of labor index for that geographic area. While most offers will be closer to the starting range, successful candidates' pay will be determined based on job-related skills, experience, qualifications, work location, internal peer equity, and market conditions. These ranges may be modified in the future.
- Region 1 $172,550 - $203,000
- Region 2 $158,950 - $187,000
- Region 3 $147,900 - $174,000
A recruiter can determine your zones/tiers based on your US location.
We are not considering candidates residing in the following states: Alaska (AK), Delaware (DE), Iowa (IA), Mississippi (MS), Nebraska (NE), South Dakota (SD), West Virginia (WV), and Wisconsin (WI)
Oura is proud to be an equal opportunity workplace. We celebrate diversity and are committed to creating an inclusive environment for all employees. Individuals seeking employment at Oura are considered without regard to age, ancestry, color, gender (including pregnancy, childbirth, or related medical conditions), gender identity or expression, genetic information, marital status, medical condition, mental or physical disability, national origin, protected family care or medical leave status, race, religion (including beliefs and practices or the absence thereof), sexual orientation, military or veteran status, or any other characteristic protected by federal, state, or local laws. We will not tolerate discrimination or harassment based on any of these characteristics.
We will work to ensure individuals with disabilities are provided reasonable accommodation to participate in the interview process, to perform essential job functions, and to receive other benefits and privileges of employment.
Disclaimer: Beware of fake job offers!
We’ve been alerted to scammers posing as ŌURA recruiters, especially for remote roles. Please note:
- Our jobs are listed only on the ŌURA Careers page and trusted job boards.
- We will never ask for personal information like ID or payment for equipment upfront.
- Official offers are sent through Docusign after a verbal offer, not via text or email.
Stay cautious and protect your personal details.
To all recruitment agencies: Oura does not accept agency resumes. Please do not forward resumes to our jobs alias, Oura employees, or any other organization's location. Oura is not responsible for any fees related to unsolicited resumes.
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Навыки
- AWS S3
- AWS Glue
- AWS Athena
- Databricks
- Dagster
- dbt
- Tableau
- CDISC
- SDTM
- ADaM
- Medidata Rave
- Castor
- REDCap
- Clinical Data Management
Возможные вопросы на собеседовании
Проверка знаний нормативной базы, критически важной для клинических данных.
Как вы обеспечиваете соответствие пайплайнов данных требованиям 21 CFR Part 11 при использовании облачных инструментов вроде AWS?
Оценка опыта работы со стандартами отрасли.
Расскажите о вашем опыте внедрения стандартов CDISC (SDTM/ADaM) в автоматизированные процессы обработки данных.
Проверка навыков проектирования систем сбора данных.
С какими основными сложностями вы сталкивались при проектировании Case Report Forms (CRFs) в EDC-системах и как вы их решали?
Оценка технических навыков в современном стеке данных.
Как бы вы спроектировали Clinical Data Repository, используя dbt и Databricks, чтобы обеспечить прослеживаемость (lineage) данных?
Проверка умения работать в кросс-функциональной команде.
Опишите случай, когда вам приходилось балансировать между требованиями регуляторов и скоростью разработки алгоритмов. Как вы нашли компромисс?
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- Страна
- США
- Зарплата
- 147 900 $ – 203 000 $