Clinical Research Coordinator I/II
Location: Onsite - Palo Alto

Key Responsibilities
Lead patient screening and recruitment efforts based on study inclusion criteria
Conduct and document the informed consent process (critical requirement)
Perform outreach to patients via phone and/or Zoom to gauge interest and obtain consent
Coordinate with clinical teams to identify eligible patients scheduled for EP procedures
Consent patients in the pre-operative setting prior to standard-of-care procedures
Support study execution during procedures where patients wear a smartwatch device
Capture detailed notes and ensure accurate data entry into sponsor systems (REDCap)
Track enrollment progress toward a goal of approximately 10 patients per month (2–3/week)

Required Qualifications
MUST have 3+ years of patient facing Clinical Research Coordinator experience
Demonstrated expertise in patient consenting and recruitment
Comfort working in a hospita...