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
Note: To make sure you don’t miss important updates from us, please check your Spam folder for emails from @celerion.com, particularly interview invitations. If you find one there, mark it as “Not Junk” to ensure future Celerion emails land in your inbox. Please note that Gmail accounts have been particularly noted as routing to Spam.
Additional Information
Company: Celerion
Location: Nebraska
Salary:
Job ID: f208abcd-4f73-47c0-8c1d-efdfb7dedf32
Specialties: Clinical Research
Required Licenses: RN, LPN/LVN
Experience Level: No Experience




