You will be responsible for performing scheduled events according to the study protocol.
You will work directly with study managers to successfully ensure a successful trial.
You will work with participants in the research process, under our care, doing vital sign checks, ECGs, blood draws and telemetry monitoring.
You will also identify and report adverse events to assist in the clinical research process.

🎯 Requirements

You will have a current NE RN or LPN license and clinical assessment skills
Your ACLS certification is a plus
Strong computer and documentation skills

🎁 Benefits

Shift: 4 x 10-hour shifts (1900-0700)
Ability to work one weekend per month
Celerion Values: Integrity, Trust, Teamwork, Respect
Equal Opportunity Employer

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