Senior Clinical Data Engineer

📋 Description

• Manage the clinical data lifecycle for a range of studies, ensuring that timelines and data integrity are upheld.

• Collaborate closely with research project managers, algorithm developers, data engineers, and external vendors to synchronize data management efforts with overall trial goals.

• Recognize data-related risks and implement strategies for mitigation, while promoting process enhancements and integrating emerging technologies as necessary.

• Direct data quality management, query analysis, optimization, deduplication, auditing, and validation within regulated data ecosystems.

• Create and supervise the design of Case Report Forms (CRFs) and electronic data capture (EDC) systems to guarantee accurate, complete, and protocol-compliant data collection.

• Establish the Clinical Data Repository that will serve as the foundation for all research and regulatory activities at Oura.

⛳️ Requirements

• 7+ years of experience in the clinical data management industry.

• Knowledge of regulations such as ICH GCP, 21 CFR Part 11, and standards like CDISC (SDTM/ADaM).

• Expertise 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 in linking clinical data management with research and enterprise practices and standards.

• Proficiency in creating dashboards using tools such as Tableau or Databricks.

• Flexibility in scheduling to facilitate calls with collaborators globally.

🏝️ Benefits

• Competitive salary and equity packages.

• Health, dental, vision insurance, and mental health resources.

• An Oura Ring for yourself along with employee discounts for friends and family.

• 20 days of paid time off plus 13 paid holidays and 8 days of flexible wellness time off.

• Paid sick leave and parental leave.