The excellent light harvesting properties and potentially low cost fabrication of organometal halide perovskites have attracted great attention in their application as solar cell device. Apart from the general advantages of organic-inorganic perovskite, CH<sub>3</sub>NH<sub>3</sub>PbBr<sub>3</sub> has a larger bandgap (~2.3eV) suitable to be the top cell in a tandem solar device. Here we use steady-state and time-resolved photoluminescence (PL) techniques to investigate the photophysical behaviour of CH<sub>3</sub>NH<sub>3</sub>PbBr<sub>3</sub> perovskite including its carrier dynamics under continuous illumination. Samples were studied under different illumination conditions and the following observations were made: (1) defect assisted recombination is dominant under low excitation under nano-second scale measurement, (2) bimolecular and Auger recombinations dominate under high excitation under the minute timescale measurement, (3) the magnitude PL decay traces decrease over time under continuous excitation. We propose that both the density of photo-generated free carriers and the density of mobile ions have an impact on the carrier dynamic of CH<sub>3</sub>NH<sub>3</sub>PbBr<sub>3</sub>. This finding provides insights into the photophysical properties of perovskite materials.