Regulatory Affairs Project Leader

Global Responsibility: Global responsibility as an RA Project Leader for designated projects Specific Responsibilities: Being the RA Project Leader and taking responsibility for all technical and scientific aspects of a biosimilar project primarily but possibly other projects as determined by the Head of Regulatory Affairs. This includes the building/preparation of the registration dossiers (both initial… Read more »

Medical Advisor

Global Responsibility Define, develop and control execution of the clinical drug development strategy and the clinical evaluation strategy, together with the scientific leadership of the commercial activities. Specific Responsibilities Lead clinical strategic global development plans through the execution and management of the biosimilar clinical trials, assuming the overall management of the clinical trials. Contribute to… Read more »