An accurate and efficient hybrid Density Functional Theory (DFT) and Multireference Configuration Interaction (MRCI) model for computing electronic excitation energies in atoms and molecules was developed. The utility of a hybrid method becomes apparent when ground and excited states of large molecules, clusters of molecules, or even moderately sized molecules containing heavy element atoms are desired. In the case of large systems of lighter elements, the hybrid method brings to bear the numerical efficiency of the DFT method in computing the electron-electron dynamic correlation, while including non-dynamical electronic correlation via the Con- v After the scaling parameters were determined using the training suite of atoms and molecules, the method was applied to carbon monoxide, boron fluoride, the bromine atom, the uranium 5+ and 4+ ions, and the uranyl (UO 2+ 2 ) ion. In all cases, the correct ordering of ground and excited states was obtained using the DFT/MRCI model. In CO, a reduction in overall error of 26% with respect to Time Dependent Density Functional Theory (TDDFT) was observed over 6 ground and excited states.A reduction in overall error of 42% with respect to TDDFT was observed in 5 ground and excited states of BF, while an accuracy with respect to experiment of 11-22% for electronic excitation energies for the first excited states of the bromine atom and uranium 5+ and 4+ ions was observed.