Clinical Research Coordinator
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4w PTO
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What you will do:
- Support Clinical Trial Managers in the day-to-day execution of clinical trials from study start-up through close-out.
- Own critical study coordination workflows such as maintaining trackers, decision logs, training matrices, and study communications.
- Ensure study documentation and training records are complete and audit-ready.
Requirements:
- 1-2+ years of full-time experience supporting clinical trials or human-subjects research in an industry or academic setting.
- Strong organizational and documentation skills with attention to detail.
- Experience with ICH-GCP, IRB requirements, or related human-subject research frameworks.
Benefits:
- Competitive salary and equity packages.
- Health, dental, vision insurance, and mental health resources.
- 20 days of paid time off plus 13 paid holidays and 8 days of flexible wellness time off.
Oura
Oura is a health technology company that produces the Oura Ring, a wearable device for tracking sleep, activity, and readiness. It is a quickly growing company with a mission-driven culture focused on employee well-being and innovation.