Clinical Research Coordinator II (Contract)
Location: Onsite
Duration: 6-month contract
Schedule: Early shift (approx. 5:30 AM – 3:00 PM)

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
Demonstrate...