The charge transfer mechanisms of ion conducting polymer materials (ICPMs) is of crucial importance both for fundamental research and for a host of practical applications, including primary and secondary batteries, fuel cells, dye-sensitized solar cells, supercapacitors and sensors. A wide variety of ICPMs has been proposed, based on: (a) different families of polymer electrolytes; (b) ionic liquids (ILs); and (c) classical ion-conducting ceramics. In these materials, the long-range charge transfer events take place owing to complex processes, which involve several possible relaxation phenomena, such as: (a) ion hopping events between ion coordination sites; (b) relaxation modes of the host matrix; and (c) polarization effects occurring at the interfaces between the different domains characterizing the materials. Broadband electrical spectroscopy (BES) is a powerful tool for the accurate investigation of the roles played by electrical relaxation events in the charge transfer processes. Indeed, BES allows to carefully detect the fundamental relaxations governing the long-range charge transfer mechanisms and to correlate them to the morphology of ion-conducting materials. This presentation overviews results of the application of BES in the study of the charge transfer mechanisms of a variety of ICMs, including: (a) polymer electrolytes based on alkaline and alkaline-earth ions; (b) pristine and hybrid inorganic-organic proton-conducting and anion-conducting membranes. The general phenomena and the fundamental theory underlying the interpretation of the events characterizing the electric response of the materials is also described. Finally, the models adopted for the interpretation of conductivity mechanisms are described and a unified conductivity mechanism is proposed.