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 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?
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
Shift:
You should be available to work 40 hours per week with the following scheduling availability:
Mon - Fri: 3x12 hour shifts - required availability (5a-7:30p) or 4x10 hour shifts - required availability 5a-5:30p). You will be scheduled a 12 or 10 hour shift within this time period.
One weekend per month
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.
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Last updated on Aug 23, 2023