The electrochemistry of a poly(vinylferrocene) (PVF) film of ca. 2100 Angstrom was investigated in 1 M aqueous NaClO4 solution with electrochemical and scanning microscopic techniques. The potential-step transients show well-defined maxima that are very similar to those found for the electrochemical switching of electronically conductive polymers, e.g., polypyrrole and polyaniline. We explore here the possibility that the film resistance accompanying changes in the polymer oxidation state is a major factor in determining the shape of these transients. These chronoamperometric curves also allow the determination of an apparent diffusion coefficient. The scanning electrochemical microscope (SECM) has been used to penetrate the PVF film and to obtain directly the thickness of the film immersed in the electrolyte solution. Different shapes of the tip current-distance curves are observed, depending on the oxidation state of the PVF film and its electrochemical treatment history. Mechanisms for the different approach curves are suggested.