Skill and experience are only the start; then the intangibles take over; flexibility, innovation, integrity. We apply these principals to our project management services around the globe and across a wide range of therapeutic indications. Integrating our deep scientific capability and our project management expertise, our goal is your success.
Celerion’s highly experienced project managers will help to successfully navigate the landscape of clinical development. Our project managers are skilled at leading, monitoring and analyzing all aspects of your trial – operations, timeline, budget and quality. They will provide expert advice and leadership of multidisciplinary drug development teams, integrating nonclinical, clinical, medical, and regulatory disciplines. We work with you from study start-up through submission of the integrated clinical study report. We become a seamless extension of your organization to execute your studies, making your R&D spend more productive.
We help you make strategy and prioritization decisions sooner and smarter, and with better information. Celerion project managers are experienced with early risk identification, which is crucial to the success of a development program. We identify those issues that are likely to be obstacles during the development process and can get you from first-in-human through proof of concept as fast as possible.
Full Service Global Clinical Development
Celerion, a full-service, early clinical CRO, is the leader in accelerating development for Phase I-IIb. Our unique combination of medical expertise, clinical operations experience and scientific excellence, enables you to make timely decisions with expert advice and high-quality data. Our leadership in clinical pharmacology through Proof-of-Concept is focused on helping you translate your science to medicine.
