Company: Moonlake
The Senior Technical Manager, Device will act as the subject matter expert responsible for all activities related to the development and PPQ (process performance qualification) for assembly of drug device combination product (DDC), functional testing of DDC to supply clinical studies and launch / commercial phase, as well as review and update the dossier in [...]Read More... from Senior Technical Manager, Device See details
The Clinical Science Specialist will provide appropriate leadership and management within Clinical Development, to provide scientific and clinical development support for products within MoonLake Immunotherapeutics assigned therapy area. Key responsibilities: Assist in protocol development in general and be fully responsible for specific sections of the protocol Provide input and participate in writing of protocol amendments [...]Read More... from Clinical Science Specialist See details
The Clinical Science Specialist will provide appropriate leadership and management within Clinical Development, to provide scientific and clinical development support for products within MoonLake Immunotherapeutics assigned therapy area. Key responsibilities: Assist in protocol development in general and be fully responsible for specific sections of the protocol Provide input and participate in writing of protocol amendments [...]Read More... from Clinical Science Specialist See details
The Senior Manager, Bioanalysis Clinical Development, provides full bioanalytical development, operational and logistical support and expertise to all parties (internally/externally) involved in MoonLake’s late stage clinical studies. Ensures the timely and efficient delivery of all bioanalytical operational aspects for clinical trials in accordance with applicable quality and regulatory standards. Major Accountabilities Acts as Bioanalytical Lead [...]Read More... from Senior Manager, Bioanalysis Clinical Development See details
The Senior Technical Manager, Device will act as the subject matter expert responsible for all activities related to the development and PPQ (process performance qualification) for assembly of drug device combination product (DDC), functional testing of DDC to supply clinical studies and launch / commercial phase, as well as review and update the dossier in [...]Read More... from Senior Technical Manager, Device See details
