Clinical Research Associate

Ceribell │ Point-of-Care EEG
Sunnyvale, CA
Category Research
Job Description
Ceribell is seeking a detail-oriented and proactive Clinical Research Associate (CRA) to join their Clinical Affairs team. The CRA will monitor clinical trials to ensure compliance with GCP, ISO 14155, and applicable regulations, focusing on medical device trials. They will be responsible for study monitoring, regulatory compliance, site management, and supporting clinical document preparation and reporting.

Requirements

  • Perform site qualification, initiation, monitoring, and close-out visits.
  • Ensure adherence to protocol, GCP, ISO 14155, and applicable regulations.
  • Verify study data accuracy and completeness.
  • Maintain knowledge of FDA and other global regulations.
  • Serve as the primary point of contact for clinical sites.
  • Provide training to site staff.
  • Manage and resolve site issues.

Benefits

  • Annual Bonus
  • Equity Opportunity
  • Health Benefits
  • Dental & Vision
  • Life Insurance
  • Long-Term Disability Insurance
  • 401(k) with matching
  • Employee Stock Purchase Plan (ESPP)
  • Cell phone stipend
  • Paid Time Off
  • Parental Leave Policy
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