Who we are looking forPurposeThe CPL is a permanent member of the cross-functional R&D global Core Team (CT) who plays a key role in defining the target disease profile (TDP), target product profile (TPP), and the development and life cycle strategies of a given project. […]
The CPL is the senior Clinical Signatory on all clinical documents related to his/her project such as phase I-IV study protocols, the Investigator’s Brochure, the Risk Assessment & Mitigation Plan, publications, and is responsible for all clinical aspects related to the Clinical Trial Dossier (clinical modules, briefing books...