Correlated metallic transition metal oxides offer a route to thin film transparent conductors that is distinct from the degenerate doping of broadband wide gap semiconductors. In a correlated metal transparent conductor, interelectron repulsion shifts the plasma frequency out of the visible region to enhance optical transmission, while the high carrier density of a metal retains sufficient conductivity. By exploiting control of the filling, position, and width of the bands derived from the B site transition metal in ABO 3 perovskite oxide films, it is shown that pulsed laser deposition-grown films of cubic SrMoO 3 and orthorhombic CaMoO 3 based on the second transition series cation 4d 2 Mo 4+ have superior transparent conductor properties to those of the first transition series 3d 1 V 4+ -based SrVO 3 . The increased carrier concentration offered by the greater bandfilling in the molybdates gives higher conductivity while retaining sufficient correlation to keep the plasma edge below the visible region. The reduced binding energy of the n=4 frontier orbitals in the second transition series materials shifts the energies of oxide 2p to metal nd transitions into the near-ultraviolet to enhance visible transparency. The A site sizedriven rotation of MoO 6 octahedra in CaMoO 3 optimizes the balance between plasma frequency and conductivity for transparent conductor performance.