Quick overview
Job description
Responsibilities
- 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.
Qualifications
- 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
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