You will provide medical supervision of ongoing trials, working closely with Clinical Operations and Medical Monitors, and support protocol amendments as needed. * In addition, you will work closely with cross-functional teams, including Clinical Operations, Regulatory Affairs, Biostatistics, and external partners, to ensure the smooth execution of clinical programs and foster a culture of scientific excellence and * You are an excellent communicator and collaborator, able to work effectively with Clinical Operations, Regulatory, Biostatistics, KOLs, and other stakeholders. * Working with free and self-determined time management, also mobile working
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