
Celerion is a leading provider of early clinical research services, specializing in Applied Translational Medicine. With over 50 years of experience and a network of global clinic beds, Celerion offers comprehensive drug development solutions including First-in-Human studies, cardiovascular safety assessments, ADME studies, and NDA-enabling pharmacology. Their expertise spans modeling and simulation, study design, biostatistics, PK/PD analysis, and bioanalytical services, ensuring robust support throughout the clinical drug development process.
Celerion is seeking a Principal Investigator to ensure the safety of subjects in clinical trials and execute studies according to protocol and regulations. This role involves reviewing protocols, managing adverse events, composing reports, and assisting with study design and training.
Celerion is a leading provider of early clinical research services, specializing in Applied Translational Medicine. With over 50 years of experience and a network of global clinic beds, Celerion offers comprehensive drug development solutions including First-in-Human studies, cardiovascular safety assessments, ADME studies, and NDA-enabling pharmacology. Their expertise spans modeling and simulation, study design, biostatistics, PK/PD analysis, and bioanalytical services, ensuring robust support throughout the clinical drug development process.