A biotech company is seeking a Clinical Trial Master File (TMF) Specialist to manage essential clinical trials and documentation. The ideal candidate will have a bachelor's degree and at least 5 years of experience in the biotech sector, including a minimum of 3 years with electronic TMF solutions. Responsibilities include ensuring quality control of documents, supporting compliance activities, and engaging cross-functionally with teams. This position is located in Allschwil, Switzerland with a hybrid working model. #J-18808-Ljbffr