If you are looking for adaptive clinical trial designs, our experienced clinical operations, pharmacology, pharmacokinetics and biostatistics teams will work with you, tailoring a solution to your unique needs. The clinical research professionals at Celerion have extensive experience and expertise in managing complex studies, helping you to transition through Proof of Concept and beyond with a particular focus on the following disease areas: vaccines oncology (over 25 indications within this complex therapeutic area), immunotherapy, infectious disease (viral or bacterial), hepatic or renal insufficiency, respiratory disease (asthma, COPD, cystic fibrosis), and other therapeutic experience including metabolism (NASH, NAFL, obesity, T2DM).
We Get Results
Celerion’s Global Clinical Development team works within a robust quality management system to ensure superior results demanded of a highly regulated industry. Our experienced project managers use proven, streamlined processes assuring you of compliance and data integrity. With Celerion’s accumulated experience of nearly 1000 studies in over 30 countries, we help you gain valuable insights from protocol development through study conduct, analysis and reporting.
We minimize your risk through early problem identification, implementation of mitigation strategies, and through close monitoring of project plans and key project and decision drivers.
Your study is executed by highly -trained and organized teams that are closely coordinated through streamlined communication and have rapid access to senior management through a flat organizational structure
Monitoring plans are tailored to each specific study, whether using our CORE
Monitoring approach, a compliance-oriented methodology taking into account each study site, deploying risk-based monitoring, or a custom solution
Enabling Early, Informed Decisions
Shaping Research for the Future Proof-of-Concept Approach for Early Answers
