Clinical Research Nurse (FT Days)

Celerion is committed to swift, exceptional clinical research through translational medicine.  Every day, we use our experience, agility, and innovative research strategies to help get drugs to market faster.   Celerion is seeking a Full-time day shift Research Nurse to assist with our clinical research trials. This is a dynamic role working with a healthy population offering the ability to learn about clinical research and see the drug development process at work.   Are you looking for an opportunity that will make a difference in the future of health care? If so, we can't wait to meet you. Do you want to learn more? Shift Mon-Sun 4x10 or 5x8 hour shifts between the hours of 5a-5:30p     If you are a Gmail user and you chose to receive e-mails from @celerion.com, please check your Spam folder regarding the status of your application, including requests for availability and interview invitations.  Additionally, ensure you mark Celerion e-mails as “Not Junk”. Celerion Values:       Integrity   Trust   Teamwork   Respect   Celerion is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, age, sexual orientation, gender identity, genetic information, marital status, qualified protected veteran status, or disability.   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.   • 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. • 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