Celerion Jobs
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Base Salary:
$38k - $38k
Base Salary:
$38k - $38k
Base Salary:
$40k
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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2010
$24.3M
659
Celerion is a global leader in early clinical research, providing comprehensive services to the pharmaceutical and biotechnology industries. Originally founded in 1933 as Harris Laboratories, the company transitioned to healthcare-focused clinical research by 1969. Celerion was established in 2010 through the acquisition of MDS Pharma Services' early-stage development operations, continuing a legacy of over 80 years in clinical research. The company specializes in early-stage clinical trials, including first-in-human studies and proof-of-concept trials. Celerion also offers bioanalytical testing, drug development consultancy, and medical writing services. With corporate headquarters in Lincoln, Nebraska, and facilities across North America, Europe, and Asia, Celerion operates over 750 beds and employs around 950 staff. The company has conducted over 6,000 clinical studies across various therapeutic areas, supporting clients in making informed decisions to advance investigational medicines from development to market approval. Celerion is committed to community engagement and workforce development, fostering local talent in biotechnology and bioanalysis.
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