Remote Clinical Research Coordinator — SaMD Trials

Ōura

United States

Remote

USD 65,450 - 90,000

Full time

14 days+
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Benefits offered by this job

Health insurance
Paid time off
Sick leave and parental leave
Employee discounts

Job summary

Ōura is seeking a Clinical Research Coordinator to join our Clinical Research Operations team. You will support day-to-day execution of regulated clinical trials across our SaMD roadmap and act as an operational partner to trial managers and researchers.

You will help ensure studies run smoothly, keep documentation inspection-ready, and provide the coordination infrastructure for high-quality evidence. Remote US role with prefered in-office 2–3 days in SF, Boston, or San Diego.

Qualifications

  • Experience supporting regulated human-subject research or clinical trials.
  • Strong documentation and record-keeping skills with audit-ready mindset.
  • Excellent written and verbal communication; collaborative team player.

Responsibilities

  • Support Clinical Trial Managers in day-to-day trial execution from start-up to close-out.
  • Maintain trackers, decision logs, training matrices, and essential document status.
  • Ensure study documents and training records are complete and current across protocols.
  • Support sponsor oversight of CROs, vendors, and sites; track deliverables and action items.
  • Collaborate with clinical research staff to maintain study records and readiness for milestones.
  • Contribute to SaMD clinical trials milestones with cross-functional partners.

Skills

Clinical trials
Documentation
Communication
Team collaboration
Organizational skills

Job description

Ōura is seeking a Clinical Research Coordinator to join our Clinical Research Operations team. You will support day-to-day execution of regulated clinical trials across our SaMD roadmap and act as an operational partner to trial managers and researchers.

You will help ensure studies run smoothly, keep documentation inspection-ready, and provide the coordination infrastructure for high-quality evidence. Remote US role with prefered in-office 2–3 days in SF, Boston, or San Diego.

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