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.
Skills Required
- Current NE RN or LPN license and clinical assessment skills
- Strong computer and documentation skills
- Availability to work evening shifts Mon–Sun 1300–2330 with one weekend per month; 5x8 or 4x10 shift patterns
- ACLS certification
Similar Jobs
What We Do
Celerion, a leader in early clinical research, delivers Applied Translational Medicine. Celerion applies our expertise and experience to translating information gained in research discoveries, to knowledge of drug action and effect in humans to support early drug development decisions and the clinical pharmacology labeling of new medicines. With over 50 years of experience and 600 global clinic beds (including 24 in-hospital), Celerion conducts and analyzes First-in-Human, clinical proof-of-concept, cardiovascular safety (TQT, robust QT), ADME and NDA-enabling clinical pharmacology studies. Celerion provides expertise on modeling and simulation, study design, medical writing (protocols and reports), clinical data sciences, biostatistics, and PK/PD analysis as well as small and large molecule bioanalytical assays through clinical drug development. Regulatory, drug development and program management complement Celerion’s service offerings. Our operations are strategically located in: Lincoln, Nebraska (Corporate Headquarters) Philadelphia, Pennsylvania Phoenix, Arizona Belfast, Northern Ireland,UK Zurich, Switzerland Vienna, Austria Richmond, Virginia Montreal, Quebec, Canada For more information, visit: www.celerion.com
