We present the electronic structure of Sr1-(
x+
y)La
x+
yTi1-
xCr
xO3 investigated by high-resolution photoemission spectroscopy. In the vicinity of the Fermi level, it was found that the electronic structure was composed of a Cr 3
d local state with the
t
configuration and a Ti 3
d itinerant state. The energy levels of these Cr and Ti 3
d states are well interpreted by the difference of the charge-transfer energy of both ions. The spectral weight of the Cr 3
d state is completely proportional to the spin concentration
x irrespective of the carrier concentration
y, indicating that the spin density can be controlled by
x as desired. In contrast, the spectral weight of the Ti 3
d state is not proportional to
y, depending on the amount of Cr doping.