About Celerion
We specialize in early clinical research and Applied Translational Medicine. Our work focuses on translating research into understanding drug action and effect in humans, supporting early drug development decisions and clinical pharmacology labeling. We have over 50 years of experience and 600 global clinic beds, including 24 in-hospital beds.
We conduct and analyze various studies, such as First-in-Human, clinical proof-of-concept, cardiovascular safety (TQT, robust QT), ADME, and NDA-enabling clinical pharmacology studies. Our services include modeling and simulation, study design, medical writing for protocols and reports, clinical data sciences, biostatistics, and PK/PD analysis. We also provide small and large molecule bioanalytical assays for clinical drug development, as well as regulatory, drug development, and program management services.
For clinical data management, we develop and administer Electronic Data Capture (EDC) databases and electronic Case Report Forms (eCRFs). This involves evaluating requirements, designing eCRFs, and ensuring high-integrity data transfers. We maintain global CDISC standards and are subject matter experts in platforms like Veeva CDMS, EDC, and CDB.
Mission & Values
We are committed to using applied translational medicine to gain insights for early drug development decisions. We apply our expertise and experience to speed up the drug development process, ensuring treatments reach patients globally.
Frequently Asked Questions
Celerion offers services in early clinical research and Applied Translational Medicine. This includes conducting First-in-Human, clinical proof-of-concept, cardiovascular safety, ADME, and NDA-enabling clinical pharmacology studies. The company also provides expertise in modeling and simulation, study design, medical writing, clinical data sciences, biostatistics, PK/PD analysis, small and large molecule bioanalytical assays, regulatory affairs, drug development, and program management. Additionally, Celerion develops and administers EDC databases and eCRFs for clinical data management.
Celerion is committed to using innovative strategies with applied translational medicine to gain insights for early drug development decisions. Its mission is to apply expertise and experience to expedite the process of bringing drugs to market, with the goal of making treatments available to patients globally.
Celerion operates in multiple locations, including Lincoln, Nebraska (Corporate Headquarters), Philadelphia, Pennsylvania, Phoenix, Arizona, Richmond, Virginia, Montreal, Quebec, Canada, Belfast, Northern Ireland, UK, Zurich, Switzerland, and Vienna, Austria.
Yes, Celerion specializes in early clinical research, specifically Phase I and Phase II studies, as well as NDA-enabling clinical pharmacology.
Celerion was founded in 2010.
Celerion is active in the Applied Translational Medicine, Global Clinical Research (phase I And Ii, Nda-enabling Clinical Pharmacology), Data Management And Biometrics, Global Bioanalytical Services (discovery Through Late Phase), Drug Development Services, and Global Clinical Development markets.
Celerion has 1001-5000 employees.
Celerion hires in 🇺🇸 United States.
Celerion is not actively hiring at the moment. Check back later for new opportunities.
Yes, Celerion is a remote-first company.
Celerion's website is www.celerion.com .
You can find Celerion on X (Twitter) and LinkedIn .
Remote companies like Celerion
Find your next opportunity with companies that specialize in Applied Translational Medicine, Global Clinical Research (phase I And Ii, Nda-enabling Clinical Pharmacology), Data Management And Biometrics, and Global Bioanalytical Services (discovery Through Late Phase). Explore remote-first companies like Celerion that prioritize flexible work and home-office freedom.
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